_:vb50950826	<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_2384>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_936> .
_:vb50950825	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
_:vb50950824	<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_2384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0043121"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A brain disease that is characterised by the presence of neurological symptoms of ophthalmoplegia, ataxia, and confusion caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, in particular thiamine (vitamin B1)."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50950826	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:190627001"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50950824 .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50950825 .
_:vb50950825	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000005> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50950826 .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.w3.org/2000/01/rdf-schema#label>	"Wernicke encephalopathy"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Wernicke's encephalopathy"@en .
_:vb50950825	<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_2384>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50950826	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SYMP_0000016> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D014899"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950824	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50950824	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/DOID_539> .
_:vb50950826	<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_2384>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:2384"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Wernicke's disease"@en .
<http://purl.obolibrary.org/obo/DOID_2384>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E51.2"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950824	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002452> .
_:vb50950825	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .