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Namespace Prefixes

PrefixIRI
n7https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0111315
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_1827
rdfs:label
idiopathic generalized epilepsy 14
wdrs:describedby
n7:doid.owl
obo:id
DOID:0111315
obo:hasDbXref
OMIM:616685
obo:hasExactSynonym
EIG14
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC12A5 on chromosome 20q13.12.