_:vb50951697	<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_3263>	<http://www.w3.org/2000/01/rdf-schema#label>	"piebaldism"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C85009"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<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_3263>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An integumentary system disease characterized by congenital absence of melanocytes in areas of the skin and hair that has_material_basis_in heterozygous mutation in either KIT or SNAI2 on chromosome 4q12 or 8q11.21, respectively."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:718122005"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:3263"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0080024"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50951697	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:2884"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Partial albinism"@en .
_:vb50951697	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E70.39"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D016116"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"PIEBALD TRAIT"@en .
<http://purl.obolibrary.org/obo/DOID_3263>	<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_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:172800"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:4344"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50951697	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50951697 .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_3263>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_16> .