SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
n3 https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n4 http://purl.obolibrary.org/obo/
wdrs http://www.w3.org/2007/05/powder-s#
rdfs http://www.w3.org/2000/01/rdf-schema#
obo http://www.geneontology.org/formats/oboInOwl#
rdf http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl http://www.w3.org/2002/07/owl#
xsdh http://www.w3.org/2001/XMLSchema#
Statements
Subject Item n4:DOID_0080461
rdf:type
owl:Class
rdfs:subClassOf
n4:DOID_0112202
n4:DOID_0050736
_:vb50940992
rdfs:label
developmental and epileptic encephalopathy 26
wdrs:describedby
n3:doid.owl
obo:id
DOID:0080461
obo:hasDbXref
GARD:12391
OMIM:616056
obo:hasExactSynonym
DEE26
early infantile epileptic encephalopathy 26
obo:hasOBONamespace
disease_ontology
n4: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.
Subject Item _:vb50940992
rdf:type
owl:Restriction
owl:onProperty
n4:IDO_0000664
owl:someValuesFrom
n4:GENO_0000147
wdrs:describedby
n3:doid.owl