<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD9CM:345.9"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_936> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:1826"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0014544"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.w3.org/2000/01/rdf-schema#label>	"epilepsy"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D004827"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:267698007"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"epilepsy syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C3020"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_FlyBase_slim> .
<http://purl.obolibrary.org/obo/DOID_1826>	<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_1826>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"EFO:0000474"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:G40.909"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1826>	<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_1826>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"epileptic syndrome"@en .
<http://purl.obolibrary.org/obo/DOID_1826>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .