<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"acquired epileptic aphasia"@en .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50950926 .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:2538"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D018887"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950926	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002488> .
_:vb50950926	<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_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0282512"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.w3.org/2000/01/rdf-schema#label>	"Landau-Kleffner syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950926	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/HP_0011463> .
<http://purl.obolibrary.org/obo/DOID_2538>	<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_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:245570"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050704> .
<http://purl.obolibrary.org/obo/DOID_2538>	<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_2538>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:6855"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50950926	<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_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:G40.8"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:230438007"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C84806"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_2538>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A childhood electroclinical syndrome that is characterized by the loss of language comprehension (auditory verbal agnosia) and verbal expression (aphasia) in association with severely abnormal electroencephalographic (EEG) findings during sleep and clinical seizures in most patients."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_2538>	<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_2538>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:98818"^^<http://www.w3.org/2001/XMLSchema#string> .