Wikidata:Property proposal/Human Phenotype Ontology ID

Human Phenotype Ontology ID edit

Originally proposed at Wikidata:Property proposal/Natural science

DescriptionThe Human Phenotype Ontology (HPO) is a widely used vocabulary of phenotypic abnormalities encountered in human disease.
Data typeExternal identifier
Domainbiology, medicine
Allowed valuesHP:([0-9]{7})
Exampleadult onset (Q21955204) -> HP:0003581
Sourcehttp://human-phenotype-ontology.github.io/about.html
Planned useWithin the next month the plan is to use this property to disambiguate phenotypic terms on wikidata related to the curation of information pertinent to NGLY1 deficiency. Much of this information is in the form of patient phenotypes - best represented using the HPO. In the near future, a bot for importing relevant nodes from the HPO is also being considered - but is not vital for this property to be useful.
Formatter URLhttp://www.human-phenotype-ontology.org/hpoweb?id=$1
See alsoDisease Ontology ID (P699), UMLS CUI (P2892), MeSH descriptor ID (P486)
Motivation

The HPO is an effective terminology for representing disease phenotypes that is now widely used. It is a member of the OBO Foundry http://www.obofoundry.org/ontology/hp.html , is used in resources like OrphaNet http://www.orpha.net/consor/cgi-bin/index.php and the 100,000 genomes initiative https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520011/ . HPO identifiers are useful, plentiful, and important for reconciling external data sources with Wikidata items. I9606 (talk) 22:24, 24 March 2017 (UTC)[reply]

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