bibliographic entry 9442867 [be/9442867]
https://w3id.org/oc/corpus/be/9442867

is a

• bibliographic reference

content

• Groza, T, Köhler, S, Moldenhauer, D, Vasilevsky, N, Baynam, G, Zemojtel, T, Schriml, L.M, Kibbe, W.A, Schofield, P.N, Beck, T. The human phenotype ontology: semantic unification of common and rare disease, Am. J. Hum. Genet, 2015, 97, 111, 124, PMID: 26119816

references

• https://w3id.org/oc/corpus/br/353717