{"id":"hp","reasoner":"none","oboSlims":false,"is_foundary":true,"ontology_purl":"http://purl.obolibrary.org/obo/hp.obo","creator":["Sebastian Koehler"],"preferredPrefix":"HP","title":"Human Phenotype Ontology","description":"The Human Phenotype Ontology (HPO) aims to provide a standardized vocabulary of phenotypic abnormalities encountered in human disease. Each term in the HPO describes a phenotypic abnormality, such as atrial septal defect. The HPO is currently being developed using the medical literature, Orphanet, DECIPHER, and OMIM. Licensed under hpo.","uri":"http://www.human-phenotype-ontology.org/","homepage":"http://www.human-phenotype-ontology.org/","mailing_list":"dr.sebastian.koehler@gmail.com","label_property":"https://www.w3.org/2000/01/rdf-schema#label","definition_property":["http://purl.org/dc/terms/description"],"synonym_property":["http://www.geneontology.org/formats/oboInOwl#hasExactSynonym","http://www.geneontology.org/formats/oboInOwl#hasNarrowSynonym","http://www.geneontology.org/formats/oboInOwl#hasBroadSynonym","http://www.geneontology.org/formats/oboInOwl#hasCloseSynonym"],"hierarchical_property":["https://www.w3.org/2000/01/rdf-schema#subClassOf"],"hidden_property":[],"base_uri":["http://purl.obolibrary.org/obo/HP_"]}