<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:300500"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_5614> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An eye disease that is characterized by reduced pigmentation of the iris and the resulting impairment of visual acuity without significantly affecting the color of skin or hair and has_material_basis in mutation in the GPR143 gene that encodes segments of the melanosomes that stores melanin."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0050633"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.w3.org/2000/01/rdf-schema#label>	"ocular albinism"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050633>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D016117"^^<http://www.w3.org/2001/XMLSchema#string> .