_:vb50942256	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://ghr.nlm.nih.gov/condition/ocular-albinism"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942256	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50942256	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007645> .
_:vb50942256	<http://www.w3.org/2002/07/owl#annotatedTarget>	"An ocular albinism that is characterized by deafness and vestibular dysfunction and has_material_basis_in digenic inheritane of a mutation in the transcription factor gene MITF on chromosome 3p13 and in the tyrosinase TYR gene on chromosome 11q14.3 that MITF regulates."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942256	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.ncbi.nlm.nih.gov/pubmed/28356565"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942256	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.ncbi.nlm.nih.gov/pubmed/29531335"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942256	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50942256	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0090100> .
_:vb50942256	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50942256	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.omim.org/entry/103470"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50942256	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007636> .
_:vb50942256	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007637> .