<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:893"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E83.01"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.w3.org/2000/01/rdf-schema#label>	"Wilson disease"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C84756"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D006527"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"hepatolenticular degeneration"@en .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Wilson's disease"@en .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_896> .
<http://purl.obolibrary.org/obo/DOID_893>	<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_893>	<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_893>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:88518009"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:277900"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<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_893>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Cerebral pseudosclerosis"@en .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0019202"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_409> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Westphal-Strumpell syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Westphal pseudosclerosis"@en .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_893>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:7893"^^<http://www.w3.org/2001/XMLSchema#string> .