Subclass of File representing sound recordings or audio tracks.
A grouping of products and/or services intentionally combined into a single offering, typically to provide added value, convenience, or specific experimental utility.
A syndromic grouping of pathogens, based on typical disease manifestation, clinical syndrome, or primary system affected. Examples include Respiratory viruses, Hemorrhagic viruses, and Gastroenteritis viruses. Clinical groups are not taxonomic categories but practical classifications used in medicine, epidemiology, and public health.
An hybridoma that provides antibodies that can be related to a pathogen.
Information on the origin of a natural part that composes the biological material.
Nucleic acid related to a pathogen. It can be extracted or synthetic.
Unpurified expression host lysate or partly purified protein
A protein as a derived product from a pathogen.
An intangible offering characterized by an activity, performance, or facilitation carried out by a provider to fulfill a user’s need.
Information on the origin of a synthetic part that composes the biological material.
Numeric code assigned to identify a particular historical version of a work (e.g. software or technical standards).
It enables managing multiple versions as first-class nodes and linking each version to its subject via evorao:versionOf and to the using resource via evorao:version (e.g., as nodes in a graph database).
Represents a specific snapshot/release of a resource (e.g., a dataset).
Subclass of File representing moving visual media, such as recordings, presentations, or movies.
Contains mycoplasmae - A protocol to remove mycoplasmae is provided
European Viral Outbreak Response Alliance Ontology
The EVORAO Ontology provides a structured and harmonized vocabulary for describing shareable pathogens as characterized biological materials, along with their derived products and associated services, organized into collections. Developed within the EVORA project, it supports consistent metadata annotation across research infrastructures, promoting findability, accessibility, interoperability, and reusability (FAIR). By aligning with relevant standards and ontologies, EVORAO facilitates cross-domain collaboration, integration, and sharing of pathogenic resources and services to enhance pandemic preparedness and response. While initially focused on virology, EVORAO is designed to be extensible and also supports metadata harmonization for other pathogens. EVORAO is compatible with DCAT, making it well-suited for efficiently cataloguing pathogen collections and related resources.
EVORAO is an ontology for standardized metadata supporting the sharing of pathogens as biological materials, their derived products, and associated services, organized into collections. While initially focused on virology, it is designed for interoperability and is extensible to other pathogens. EVORAO is compatible with DCAT, making it well-suited for efficiently cataloguing pathogen collections and related resources.
A collection of operations that provides access to one or more datasets or data processing functions.
Protein that can bind to certain types of foreign bodies, such as pathogens.
The level of biocontainment required or applied in the facility where the biological agent is manipulated.
The Biosafety Level (BSL) reflects the operational safety measures implemented, which may differ from the intrinsic risk defined by the agent’s Risk Group (RG).
Using a dedicated data provider for BSL instances is recommended. Definitions of existing Biosafety Levels can also be found at wd:Q18396533, wd:Q18396535, wd:Q18396538, and wd:Q18396539.
Assurance given by an independent certification body that a product, service or system meets the requirements of a standard.
Set of products and services with some common characteristics.
Subclass of File representing structured or unstructured datasets, often used for analysis, storage, or transfer of information.
A reference to an expression vector plasmid, typically embedding a resistance marker for inducible protein expression.
A reference that permits to retrieve an item from an external provider.
A program, grant, or project providing financial support for the access or use of a product or service, either fully or partially.
The corresponding International Air Transport Association (IATA)'s category for dangerous goods that are transported by air.
The IPLC area (Indigenous People and Local Communities) from which a physical item originates.
Host organism from which the pathogen was isolated.
Periodical journal publishing scientific research.
A term or phrase used to tag and categorize content.
A Material Safety Data Sheet (MSDS) or Safety Data Sheet (SDS) is a standardized document that contains crucial occupational safety and health information related to the product.
The individual or organization responsible for the original discovery, isolation, or creation of an item, providing information about the source or origin of the sample.
A collection of distinguishing information that enables the differentiation of a pathogen from another.
Identifier for 3D structural data as per the PDB (Protein Data Bank) database.
The process of identifying cells that have successfully incorporated a plasmid, typically using antibiotic resistance markers.
A population of cells that originates from a primary culture, adapted to grow and divide under laboratory conditions. Used in biotechnology to consistently produce biological substances.
The organism used to grow and multiply the pathogen under controlled conditions.
A provider of products or services, as a specific organization.
Risk group classification guides initial handling of biological agents in labs but doesn't systematically equate to biosafety levels. Actual risk varies with the agent, procedures, and personnel competence.
The Risk Group (RG) assignments to an item are jurisdiction-dependent and may differ between countries/regions and by material form (e.g., live isolate, inactivated preparation, nucleic acid). Assignments can also change over time. We store here a single reference assignment; users must verify the current, locally applicable assignment with their competent authority.
Using a dedicated data provider for Risk Group instances is recommended. Definitions of existing Risk Groups can also be found at wd:Q125449389, wd:Q125449412, wd:Q125449429, and wd:Q125449439.
Distinctive attributes of a product that set it apart from other similar items e.g., Reference strain, Vaccinal strain, Antiviral resistant strain ...
These special features help researchers and professionals in the field to select appropriate virus strains for their specific research needs and applications.
The process by which the pathogen spreads between hosts.
An organism with one or more new mutations is referred to as a “variant” of the original organism if not sufficiently different to be termed a distinct strain.
A virus vernacular name or a name that describes a group of viruses.
A subset of words or phrases specific to a particular subject or field.
Any category apart from its main category in which this product or service can fit.
A method used to determine the specificity, affinity, or functionality of an antibody or antiserum.
Details the origin of one or more unitary parts that make up the biological material. In the case of recombinant biological material, multiple parts may be involved.
It can be multiple parts in case of a recombinant biological material.
Any certification related to the current product or service; e.g., ISO certification.
The document(s) issued by an authority certifying the conformity of the subject to the applicable scheme, including, as the case may be, the documents attesting the equivalence to another certification scheme.
Identifies other viruses that may co-infect the host organism along with the primary virus, indicating the presence of multiple viral infections within the same host.
The collection(s) to which belongs this item.
Any additional documents that provide supplementary information, instructions, or guidelines relevant to the use of this item.
Any equivalent taxon in a different taxonomy if exists/known to serve as a bridge (e.g, ICTV towards NCBI).
Could serve as a bridge between ICTV and NCBI as several providers currently uses NCBI Taxonomy.
A reference that permits to retrieve another related item from an external provider.
A program, grant, or project providing financial support for the access or use of the product or service, either fully or partially.
Links a product or service to one or more financial mechanisms, initiatives, or grants that enable or support its provision or access.
A GenBank formatted file that contains detailed sequence and annotation information of a nucleic acid construct.
Indication of the possible host(s) for the identified pathogens among the listed main categories.
The host organism from which the pathogen was originally isolated.
Specifies the constituent products and/or services that are part of the bundle.
List of terms used to tag and categorize this Item.
An ordered list of textual taxon names representing the taxonomic lineage of the current taxon, normally from the highest known ancestor to the immediate parent.
This property is intended for display, indexing, and search optimisation purposes. It represents a denormalised view of the taxonomic lineage and is typically derived automatically from successive parentTaxon relations. It MUST NOT be considered authoritative for taxonomic reasoning. This property provides a flattened, display-oriented view of the lineage and does not replace the parentTaxon relation.
The research infrastructure of which this organization is a member.
The identification of the pathogen or group of pathogens (e.g; name, taxon identification, etc.) related to the current item.
The pathogen identification contains information about name and taxon but in some cases(e.g: FAIRSHARING) there may have no direct pathogen related but simply a taxonomic information .... the default value should be the root of virology: Viruses.
Specific selectable markers in the plasmid, such as antibiotic resistance genes, used to identify and maintain cells that contain the plasmid.
Any historic version of this taxon having a different name.
The cell line used for the production or propagation of the pathogen, detailing the cellular environment employed in its cultivation and study.
The host organism that propagates the pathogen.
Identifies the type of entity (ontology class) described by the response to a query. Values should be expressed as IRIs (e.g., from an ontology).
This property defines what the response is about, independent of its serialization.
Values should be ontology class IRIs (e.g. https://w3id.org/evorao/Virus).
Resource published or curated by a single agent.
The related standard operating procedure file (SOP).
The potential geographical or environmental source from which the pathogen is believed to have originated or been transmitted.
The method or route through which the pathogen is transmitted from one host to another, detailing the mechanisms of infection spread.
Refers to the classification of a protein based on the specific type of functional analysis performed to determine its biological activities and roles. Possible values include 'Enzymatic' (the protein has been characterized for its enzyme activity) and 'Antigenic' (the protein has been characterized for its ability to elicit an immune response).
Date of formal issuance (e.g., publication) of the resource.
encoded using the relevant ISO 8601 Date and Time compliant string [DATETIME].
Most recent date on which the resource was changed, updated or modified.
An aditional information as a textual comment.
A curated collection of metadata about resources.
The URL template that allows to get the content.
A keyword or tag describing the resource.
A web page that serves as the main or introductory page.
A unique string identifier assigned to a digital object, providing a permanent link for reliable citation and access. The Digital Object Identifier (DOI) is a persistent identifier that is an ISO standard.
The specific location or region where a physical item, originates or is naturally found.
geonames.org API is a service data provider to consider as suggested by DCAT-AP.
The legal terms and conditions under which the subject can be used, shared, or distributed, indicating any restrictions or permissions.
A reference that permits to retrieve the sequence information from a sequence provider.
A work on making it a subclass of External related reference might be consistent and beneficial for data structuration but special attention will have to be take to ensure it remains consistent with the actual the use cases for users.
The name of the DNA coding sequence or corresponding peptide/protein sequence fused to a sequence of interest, used to facilitate experimental operations such as purification, detection, localization, tracking, solubility enhancement, or selection. Applicable to both proteins and nucleic acids.
This class is used for controlled vocabulary terms (e.g., His Cterm, His Nterm, MBP, GST, Strep, FLAG-Tag, SUMO ...) and not the literal sequences.
The possible taxonomic ranks and their description.
A structured representation of data about the classification and naming of biological organisms into groups according to shared characteristics.
The URL that permits to access to the product/service detailed description page on the provider's website and/or allows to place an order about it or at least describe the process to place an order/enquiry.
Indicate if the biological part was produced with access to a physical genetic resource.
The sequence ID that permits to retrieve the sequence information from the sequence provider.
Guidelines for safely managing spills or leaks of the product, including containment, cleanup procedures, and precautions to prevent harm to people, property, and the environment.
The locality in which the street address is, and which is in the region. e.g, the city.
The region in which the locality is, and which is in the country. For example, California or another appropriate first-level Administrative division.
Two-letter country codes from ISO 3166-1 alpha-2.
An alternate text for the image, if the image cannot be displayed.
A statement summarizing observed characteristics, behaviors, or findings derived from the antibody characterization process.
Indicates whether or not if the antibody was purified by affinity.
Information describing the molecular or antigenic specificity of the antibody, including its recognized target(s), cross-reactivity with related antigens, and any contextual information supporting its selectivity.
The specification of the class of antibody based on its production method or biological origin. Expected values are "Polyclonal", "Monoclonal" or "Serum"
The state or condition in which this item is accessible and ready for use or can be obtained.
Possible availabilities may differ from a project to another.
Indicates whether the biological material includes any part originally collected from a natural source (true) or is composed exclusively of synthetic parts (false).
It makes sense that only recombinant biological materials can have a mixed material origin! Mixed origin (natural + synthetic) is represented by EVORAO:recombinantMaterial = true and EVORAO:biologicalSourceType = true, together with both EVORAO:NaturalPartOrigin and EVORAO:SyntheticPartOrigin instances linked via EVORAO:biologicalPartOrigin
Information about guidelines and regulations designed to prevent the exposure to or release of potentially harmful biological agents. It thereby contributes to protecting people and the environment from biohazards while accessing this product or service.
Indicates if the current service or product can be used to produce GMO.
It is recommended to have a value for this field, no value will be understood as unknown.
Details about the clinical aspects of the pathogen, including symptoms, severity, treatment protocols, and patient outcomes.
The plasmid into which the nucleic acid has been cloned.
Specification of the terms and parameters for transporting.
Set to TRUE if a proxy date for the collection date is used.
The provider of the data of the collection.
The date when the sample was collected in situ. If unknown/private, use a proxy date such as 'date received' and indicate this by setting to true the before date property.
Indicates whether the sample contains contamination with co-infecting viruses. Possible values are ‘Not tested’, ‘Contaminated’, and ‘No contamination detected’.
When it can be assessed, it is recommended to indicate whether contamination with co-infecting viruses was detected or if the test was not performed.
The content type of the response to queries. It specifies the serialization, file type, or media type used to convey the resource, typically expressed as a MIME type following IANA media type registrations.
This property characterizes how the content is structured or encoded, independent of the entity type it represents.
Values should use MIME types (e.g. application/json, text/csv, text/tab-separated-values, text/x-fasta, application/vnd.genbank).
The web address or location where the file content is stored and can be accessed or downloaded.
The geographical location where the sample was collected in situ. Used for Nagoya/CBD; equivalent to 'country of origin'.
The ability of the pathogen to be cultivated or grown in laboratory conditions. Possible values are 'Cultivable pathogen', 'Uncultivable pathogen' or 'Inactivated pathogen'.
Might also be related to a product sub-category that helps filtering.
description of modification(s) made from the reference sequence(s)
List the modifications mades from the reference sequence if any.
Guidance on the safe and environmentally responsible disposal of the product, including recommended disposal methods, regulatory requirements, and precautions to avoid harm to people and the environment during disposal.
A distinct structural and functional unit within the protein, often capable of independent folding and stability, which contributes to the protein's overall function.
Details the potential environmental impact of the product, including its effects on ecosystems, persistence, degradability, bioaccumulation potential, and toxicity to aquatic and terrestrial organisms.
Conditions under which individuals or organisations may benefit from the financial mechanism, including access rules, eligibility requirements, or geographical/institutional restrictions. May be expressed as text or as a link to a formal eligibility statement.
Keep clear and user-friendly; provide a link if criteria are complex.
Specifies measures to limit exposure to the product, including recommended engineering controls (e.g., ventilation) and personal protective equipment (PPE) such as gloves, masks, goggles, and clothing to ensure safe handling.
Refers to the form in which the protein is produced and manifested in a biological system. Possible values include 'Soluble' (proteins that are dissolved in the cellular or extracellular fluid) and 'Inclusion bodies' (aggregated proteins that are insoluble and form within the cell).
The host organism or cellular environment used to produce a protein from a specific gene. Possible values include 'E. coli' (bacterial system), 'Insect cells' (using baculovirus vectors), and 'Mammalian cells' (mammalian cell lines).
Guidance on how to safely extinguish a fire involving the product, including suitable extinguishing agents, special protective equipment for firefighters, and any specific hazards from combustion.
Instructions on immediate actions to take in case of exposure to the product, including inhalation, ingestion, skin, or eye contact. This section outlines steps to minimize harm before medical help is available.
The file type or format that indicates how the data within the file is structured.
Detailed information about the specific biological functions, mechanisms of action, and technical attributes of a protein. This includes how the protein interacts within biological systems, its role in cellular processes, and any relevant technical details such as structure, activity, and interactions with other molecules.
The process of determining and describing the specific biological activities and roles of a protein. Possible values include 'Functionally characterized' (the protein's functions have been identified and described) and 'No functional characterization' (the protein's functions have not been identified or described).
The organization providing the financial support.
The date on which the financial mechanism ceases to apply to the supported product or service.
The date from which the financial mechanism is active or applicable to the supported product or service.
Identifies the overarching financial framework, research initiative, or support mechanism that enables or contributes to the provision of a product or service. The value may correspond to a European funding framework (e.g. Horizon Europe), a specific research initiative (e.g. an EU project), or another public or private funding mechanism.
Provides any additional details or clarifications not covered in other sections of the MSDS, such as references, supporting documents, or specific instructions for safe handling and use of the product.
The extent of the pathogen's genetic material that has been sequenced, with possible values including 'Complete genome' for the entire genome, 'Complete coding sequence' for all coding regions, and 'Partial sequence' for only a portion of the genetic material.
Genotype information that identifies organisms that cluster in phylogenetic trees, thus different clusters are distinct genotypes.
A formal reference or agreement number assigned by the funding body.
Instructions on the safe handling practices and storage conditions for the product, including precautions to prevent accidents, degradation, or contamination, as well as recommended temperature, humidity, and container requirements.
Outlines the potential risks and dangers associated with handling the product, including its physical, chemical, and health hazards. This section provides information on toxicity, flammability, reactivity, and other relevant risks for safe use.
The corresponding International Air Transport Association (IATA)'s category for this Product.
Refers to the state of aggregated proteins within a cell. Possible values include 'Denatured' (proteins are in an unfolded, inactive state) and 'Refolded' (proteins have been processed to regain their functional, active conformation).
indigenous people and local community origin
The specific IPLC area (Indigenous People and Local Communities) from which this sample/element was sampled, if relevant.
Non cultivable sample, infectivity cannot be tested
Indicates the ability of the pathogen to establish an infection in a host organism, with possible values detailing whether infectivity has been tested, quantified, or cannot be tested due to non-cultivable nature.
The description of the completed infectivity test, providing details on the methods, conditions, and results of the test used to assess the pathogen's ability to infect a host organism.
Any reference or indication to be used for local retrieval purpose.
Identifier given to a pathogen that has been isolated from an infected host and propagated in a laboratory culture. The isolate information may include an internal reference code from the laboratory that took the sample or performed the isolation, as well as details about the specific conditions of isolation, such as the name of the town, hospital, and type of host.
The environmental and procedural conditions under which the pathogen was isolated.
The specific method or procedure used to isolate the pathogen from a host organism or sample, detailing the techniques and tools employed in the isolation process.
The scientific journal in which the publication was published.
Indicate whether a Letter of Authority is required, confirming the necessity of formal authorization. The possible values are 'Not applicable', 'Not required', 'Required for customers in the EU' or 'Required'.
When a letter of authority may be required, as is often the case for certain pathogens such as plant viruses, it is strongly recommended to indicate the status of this requirement, as this information may affect delivery conditions and is important for the end-user.
A text or html code that provides any related data sharing licence and/or attribution.
The http request method used to acces the login request url.
The name of the token, unique identifier of an interaction session, that will have to be reused as credential in the query.
The URL template that allows to log in if required.
The designated contact point responsible for providing information related to the safety, handling, and regulatory compliance of the biological product.
The MSD is a document that provides detailed information about the properties, hazards, handling, storage, and emergency procedures related to the use of a chemical or substance.
The species of the infected organism in the experiment.
The specific name of the infected organism, including its modification if necessary.
modifications from the reference sequence(s)
Set to TRUE if there was is any modification made from the reference sequence.
Indicates if the current nucleic acid has No mutation compared to the reference sequence if the value is set to false or if it contains mutations (no frameshift, no unexpected STOP codon) if set to true.
Except for non-sequenced nucleic acids, for which mutations cannot be assessed, it is strongly recommended to determine whether any mutations are present in the provided sequenced nucleic acid.
Indicates whether the sample contains mycoplasma contamination. The possible values are 'Not tested', 'Mycoplasma free', 'Contains mycoplasmae', 'Contains mycoplasmae - A protocol to remove mycoplasmae is provided'
When it can be assessed, it is recommended to indicate whether mycoplasma contamination was detected or if the test was not performed.
The specific mutations that have been identified and documented in the nucleic acid sequence.
An overarching category that encompasses the current category within a hierarchical classification system. It serves as the top-level classification, organizing related subcategories under its umbrella to create a structured and logical order.
A short designation of this recombinant part of the related biological material.
The number of times the pathogen was cultured through serial passage, a process used to increase the stock but which can also lead to the evolution of the original pathogen.
A pathogen common name or a name that describes a group of pathogens.
Identification of the specific type of pathogen among the listed categories e.g. 'Virus','Viroid','Bacterium'...
Reference of the permit identifiers for access to the genetic resource, applicable if the genetic resource falls under Access and Benefit-Sharing (ABS) regulations.
physical and chemical properties and information on ingredients
Key characteristics of the product, such as physical state, appearance, solubility, pH, chemical composition, and molecular weight, essential for safe handling and storage.
The technique, method, or procedure employed to obtain or prepare the material prior to its use or storage.
The biological and technological methods and processes used to produce the antibody.
Refers to the degree of purity achieved for a protein sample. Possible values include '>95%' (the protein is highly purified, with more than 95% purity) and 'Unpurified expression host lysate or partly purified protein' (the protein is either unpurified and present in the host cell lysate or only partially purified).
A provider of this product or service, as a specific organization.
Information that permits to assess the quality level of what will be provided.
The http request method used to access the requested query url.
The data provider for the description of the taxonomic ranks used in this taxonomy.
Indicates if this biological material is a recombinant biological material.
Information not required if the current biological part constitutes the complete biological material.
The reference or the stock keeping unit of the service or item provided in the provider's catalogue.
The identifier reference of the connected external item.
The label informing what this reference is about.
The url prefix that once completed with the reference will lead to the linked external resource.
The specific region encompassed in the product.
The regionEncompassedInThisProduct property is strongly recommended for cloned nucleic acids, as it provides essential information that greatly improves the clarity and precision of the description for the user.
Lists applicable laws, regulations, and standards governing the product, including local, national, or international requirements for its handling, use, transportation, and disposal, ensuring compliance with legal obligations.
The highest risk group related to this resource. The risk group of a biological agent guiding its initial handling in labs according to the risk group classification defined by the WHO laboratory biosafety manual.
The corresponding organization's persistent identifier from the Research Organization Registry (ROR).
Tell whether or not the sequence of the product was controlled, which is expected for sequenced nucleic acids and especially important for cloned ones.
For non-sequenced nucleic acids, the sequenceChecked value cannot be assessed. In all other cases, it is strongly recommended to indicate whether the sequence verification has been performed or not. For cloned products in particular, providing this information is especially meaningful, as sequence verification is a key element in confirming the integrity of the cloned construct and is therefore expected to be documented whenever available.
Textual encoding of a biological sequence information in FASTA format.
In FASTA format the line before the nucleotide sequence, called the FASTA definition line, must begin with a charater ('>'), followed by a unique SeqID (sequence identifier).
In cases where no reference sequence exists in public repositories, the corresponding FASTA sequence is expected; otherwise, the reference sequence is sufficient. In case the sequence is made of multiple parts several fasta sequences can be provided.
The name of the sequence provider within the list of accepted sequence providers.
Refers to the level of sequencing performed on the nucleic acid. Possible values include 'Not sequenced' (no sequencing has been performed), 'Partly sequenced' (only a portion of the nucleic acid sequence has been determined), and 'Fully sequenced' (the entire nucleic acid sequence has been determined).
Genetically related pathogens that group together based on serological relationships.
Details on the ability of a detection kit to correctly identify negative results, distinguishing between the target analyte and other substances without cross-reacting.
Describes the product’s stability under normal conditions and its potential to react with other substances. This section includes information on hazardous reactions, conditions to avoid, and incompatible materials that could cause degradation or dangerous reactions.
Specifies the conditions under which the product has to be stored to maintain stability and integrity, such as temperature, buffer, and other environmental factors.
e.g, could be a xsd:string in enumeration ('Freeze Dried', 'Liquid Nitrogen', 'Viral Storage Medium -20C', 'Viral Storage Medium -80C', 'Living plant material (>= +4°C)', 'Gas Phase', 'Ethanol -20C', 'Ethanol -80C', 'Dried').
Identifier given to a genetic variant within a single species.
The building/apartment number and the street name.
The subspecies information differentiates closely related pathogens within a single species.
Indicates the presence and condition of a tag on the protein after solubilization. Possible values include 'Uncleaved Tag' (the tag is still attached to the protein), 'Cleaved Tag' (the tag has been removed from the protein), and 'No Tag' (the protein does not have a tag).
Specific molecular structure or epitope recognized and bound by an antibody.
The specific area or sequence within the target analyte that the detection kit is designed to identify and interact with, ensuring accurate detection and analysis.
The data provider for the taxons of the taxonomy.
The taxonomic identifier as a persistent identifier accross releases.
The taxonomic_Node Identifier as an identifier specific the current taxon in the corresponding release/version of the taxonomy.
NCBI does not have a taxon_node id, only a taxonomicID. Taxon_node id is Unique in ICTV= Key of the taxon node!
Expert advice or guidelines provided to ensure the optimal use, performance, and maintenance of what is provided, including best practices, troubleshooting tips, and procedural instructions.
An external API or Endpoint that permits to retrieve the terms of this vocabulary.
Indicates whether the biological material can be distributed without restriction to third parties, as indicated by the ABS permit, in case an ABS permit is required.
Details on the potential health effects of the product, including routes of exposure (inhalation, ingestion, skin, eye contact), acute and chronic toxicity and symptoms of exposure.
Details the regulations and guidelines for safely transporting the product, including classifications for road, air, sea, or rail transport, UN numbers, packaging requirements, and any special precautions to ensure safe transit.
The cost per access for one unit as defined by the unit definition.
The cost per access may not always be defined as a fixed numerical value. In some cases, the price is conditional or available only upon request. To accommodate such cases, descriptive information should be provided through the property EVORAO:unitCostNote (xsd:string). This allows handling of cost statements such as “on request,” “depends on volume,” or “free access for academics,” which cannot be captured by a simple numeric value.
The currency in which the unit cost is expressed, following ISO 4217 three-letter codes (e.g., EUR, USD).
A free-text note describing special conditions or cases where the cost cannot be represented by a numerical value (e.g., on request, free for academics, depends on volume).
A short description of what will be delivered by ordering one unit of this item.
The description of what will be delivered to the end-user (e.g.: packaging, quantity...).
Specifies any limitations or conditions on the use of the biological material, including restrictions on research, commercial use, or distribution, considering any potential concerns about the related genetic material.
The data provider for the Version ID of this taxonomy.
Identifier of what type of entities the version qualifies.
A collection of data, published or curated by a single agent, and available for access.
A collection of data that this data service can distribute.
This property rather intends to point towards Catalogues as collections of Datasets.
The main category of the service or product.
Information about the origin of the biological material, compulsory for access, utilization, and benefit-sharing of genetic resources in compliance with the Nagoya Protocol.
Information on the origin of a unitary, cohesive part that is part of, or constitutes the biological material. It can be multiple parts in case of a recombinant biological material.
Vernacular name that is the name used in everyday language to refer to something like an organism or group of organisms. This name is typically easier to remember and pronounce compared to the scientific or technical name.
Subclass of File representing textual or written files such as reports, manuals, or forms.
A Digital Object Identifier (DOI) that can be related.
The name of the origin from which knowledge is obtained. This can include any entity that provides information.
The taxonomy release(s) in which this entity exists.
Entity serving as focal point of information.
A nucleic acid or protein sequence information.
Relative level or position of the identified taxon in the taxonomy.
The entity responsible for making the resource available.
Resources of type foaf:Agent like EVORAO:PersonOrOrganization are recommended as values for this property.
Use of Data provider recommended. It serves as a local cache for ISO3166.
Biological entity that causes disease in its host, which is typically an infectious microorganism or agent, such as a virus, bacterium, protozoan, prion, viroid, or fungus.
A tangible, physical item made available by a provider for use, consumption, or ownership transfer.
A term used to classify a group of products that share common characteristics or functions, which helps in their organization.
An offering provided by a provider, which may be tangible (a product) or intangible (a service).
part of wd:Q2897903 (goods and services ).
A method or procedure used to detect, identify, and confirm the presence of a specific nucleic acid sequence, pathogen, or associated constructs. This may involve various techniques such as PCR, sequencing, hybridization, or other molecular methods, utilizing specific tools and procedures for accurate detection and analysis.
Unique persistent identifier for a person, provided by the Open Researcher and Contributor ID (ORCID) organisation.
The web address or location where the details or content is stored and can be accessed or downloaded.
Boolean value indicating whether the specificity of the product has been formally documented.
The tagSequence is strongly recommended for cloned nucleic acids and proteins but may be absent in certain cases, such as for some non-cloned nucleic acids.
The titer value, its corresponding unit, and the method of quantification (e.g., RT-qPCR, TCID50), representing the concentration or amount of unit present in the sample. The titer corresponds to the highest dilution factor that still yields a positive reading.
A numerical value indicating relative importance or priority, generally processed in ascending order. This weight helps prioritize content when organizing or processing data. Its value can be negative, with a default set to 0.
The lowest weighted Data providers are triggered first.
This property may be usefull to populate at first entities that are referenced by others (e.g. Version ahead of Rank ahead of Taxon).
An information that allows someone to establish communication.
A social entity established to meet needs or pursue specific goals.
Digital document or record stored in a specific format that contains data or information.
Subclass of File representing visual content such as pictures, diagrams, or illustrations.
Scientifically classified group or entity within the reference taxonomy.
The taxon of the highest rank known that can be used to classify a pathogen or group of pathogens (e.g viruses) in the reference taxonomy.
Information about terms and conditions under which the subject can be used, shared, or distributed, indicating any restrictions or permissions.
The related sequence information from a sequence provider or in fasta format.
Sequence information is logically one of the minimal quality requirements for entities such as pathogens, nucleic acids, and proteins, and should always be provided. However, in some rare cases, a nucleic acid may still be valuable even if it has not been sequenced after being extracted from identified material. In such exceptional cases, the sequence may legitimately be missing.
The version indicator (name or identifier) of a resource.
A word or set of words used to identify and refer to an entity.
Information about the origin of the biological material, essential for access, utilization, and benefit-sharing of genetic resources in compliance with the Nagoya Protocol.
International Resource Identifier (IRI) that uniquely identifies or refers to the resource. IRIs include URIs, and URIs include URLs.
An IRI is a global identifier standardized by IETF RFC 3987. It may or may not be resolvable on the web. IRIs include URIs, and URIs include URLs.
An external API (Application Programming Interface) or Endpoint that permits to retrieve data from other sources.
Conceptual entity that groups one or more populations of an organism or organisms, as seen by taxonomists, to form a unit.
The taxonomic taxons connected to their parent so that a full lienage can be rebuild.
Any other name under which the entity can be known.
This includes previous names, acronyms, former taxonomic terms, and other variations.
This information can serve as keywords for search purposes and as a bridge with other projects that use different naming systems or taxonomies.
A unique identifier of the resource being described or cataloged.
The identifier is a text string which is assigned to the resource to provide an unambiguous reference within a particular context. Persistent identifiers should be provided as HTTP URIs.
E.g. for virus products it should basically be based on the following Pattern: 'Virus name', 'virus host type', 'collection year', 'country of collection' ex 'suspected epidemiological origin', 'genotype', 'strain', 'variant name or specific feature.
The title of the item should be as short and descriptive as possible.
Word or phrase from a specialized area of knowledge.
A short explanation of the characteristics, features, or nature of the current item.
Describe this item in few lines. This description will serve as a summary to present the resource.