SPARQL | HTML Microdata document
This HTML5 document contains 16 embedded RDF statements represented using HTML+Microdata notation.
The embedded RDF content will be recognized by any processor of HTML5 Microdata.
Namespace Prefixes
Prefix IRI
n7 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_0080425
rdf:type
owl:Class
rdfs:subClassOf
_:vb50940920
n2:DOID_0112202
n2:DOID_0050736
rdfs:label
developmental and epileptic encephalopathy 47
wdrs:describedby
n7:doid.owl
obo:id
DOID:0080425
obo:hasDbXref
OMIM:617166
obo:hasExactSynonym
early infantile epileptic encephalopathy 47
DEE47
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A developmental and epileptic encephalopathy characterized by onset in the first days or weeks of life of intractable seizures, developmental regression after seizure onset, intellectual disability, and neurologic impairment that has_material_basis_in heterozygous mutation in the FGF12 gene on chromosome 3q28.
Subject Item _:vb50940920
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000147
wdrs:describedby
n7:doid.owl