SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
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n2 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 n2:DOID_0112202
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050701
rdfs:label
developmental and epileptic encephalopathy
wdrs:describedby
n6:doid.owl
obo:id
DOID:0112202
obo:hasDbXref
OMIM:PS308350
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An electroclinical syndrome characterized by epileptiform activity and at least one other pathology that together contribute to cognitive and behavioral impairments including developmental delay or regression with onset anywhere from birth to adulthood.