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Namespace Prefixes

PrefixIRI
n6https://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#
n8http://purl.obolibrary.org/obo/doid#
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_0080422
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0112202 _:vb50940916 n2:DOID_0050736
rdfs:label
Dravet syndrome
wdrs:describedby
n6:doid.owl
obo:id
DOID:0080422
obo:hasAlternativeId
DOID:0060171
obo:hasDbXref
ORDO:33069 OMIM:607208 GARD:10430
obo:hasExactSynonym
severe myoclonic epilepsy of infancy developmental and epileptic encephalopathy 6 early infantile epileptic encephalopathy 6 DEE6
obo:hasOBONamespace
disease_ontology
obo:inSubset
n8:DO_FlyBase_slim
n2:IAO_0000115
A developmental and epileptic encephalopathy characterized by onset of seizures that are usually refractory to treatment in the first year of life after normal early development and impaired psychomoter development starting around the second year of life that has_material_basis_in heterozygous mutation in the SCN1A gene on chromosome 2q24.
Subject Item
_:vb50940916
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n6:doid.owl