SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
n6 https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
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_0080448
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0112202
_:vb50940966
n2:DOID_0050737
rdfs:label
developmental and epileptic encephalopathy 48
wdrs:describedby
n6:doid.owl
obo:id
DOID:0080448
obo:hasDbXref
OMIM:617276
obo:hasExactSynonym
early infantile epileptic encephalopathy 48
DEE48
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A developmental and epileptic encephalopathy characterized by seizure onset before 1 year of age, global developmental delay, intellectual disability, absent speech, and minimal or absent motor development that has_material_basis_in homozygous or compound heterozygous mutation in the AP3B2 gene on chromosome 15q25.
Subject Item _:vb50940966
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000148
wdrs:describedby
n6:doid.owl