_:vb50940992	<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_0080461>	<http://www.w3.org/2000/01/rdf-schema#label>	"developmental and epileptic encephalopathy 26"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940992	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/IDO_0000664> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A developmental and epileptic encephalopathy characterized by onset in the first years of life of seizures, developmental delay, intellectual disability, poor speech, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the KCNB1 gene on chromosome 20q13."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"DEE26"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<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_0080461>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0080461"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"early infantile epileptic encephalopathy 26"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0112202> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:12391"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:616056"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50940992	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/GENO_0000147> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050736> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50940992 .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0080461>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50940992	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .