<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
_:vb50948307	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50948309	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50948307	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0019173> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:7862"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C85218"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:364.24"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948311	<http://www.w3.org/1999/02/22-rdf-syntax-ns#first>	<http://purl.obolibrary.org/obo/UBERON_0000014> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50948309	<http://www.w3.org/2002/07/owl#intersectionOf>	_:vb50948311 .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.w3.org/2000/01/rdf-schema#label>	"Vogt-Koyanagi-Harada disease"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948308	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50948307	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:44923005"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50948310	<http://www.w3.org/1999/02/22-rdf-syntax-ns#first>	<http://purl.obolibrary.org/obo/UBERON_0002384> .
_:vb50948311	<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_12297>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:12297"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948308	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004026> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:H20.82"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948310	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50948308	<http://www.w3.org/2002/07/owl#someValuesFrom>	_:vb50948309 .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Harada's disease"@en .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"uveomeningoencephalitic syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0060039> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D014607"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50948307 .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50948308 .
_:vb50948310	<http://www.w3.org/1999/02/22-rdf-syntax-ns#rest>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#nil> .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0042170"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948307	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50948311	<http://www.w3.org/1999/02/22-rdf-syntax-ns#rest>	_:vb50948310 .
_:vb50948308	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
_:vb50948309	<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_12297>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Vogt-Koyanagi syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_12297>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An autoimmune disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis."^^<http://www.w3.org/2001/XMLSchema#string> .