<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50936839	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0271097"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D052245"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.w3.org/2000/01/rdf-schema#comment>	"Xref MGI.\nOMIM mapping confirmed by DO. [LS]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050737> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:7843"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0050439"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A syndrome characterized by a combination of hearing loss and visual impairment."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:PS276900"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936839	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000148> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<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_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C85217"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936839	<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_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:886"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_225> .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50936839 .
<http://purl.obolibrary.org/obo/DOID_0050439>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:57838006"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50936839	<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_0050439>	<http://www.w3.org/2000/01/rdf-schema#label>	"Usher syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .