@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_head {
  this: np:hasAssertion dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_assertion ;
    np:hasProvenance dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_provenance a np:Provenance .
  dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_assertion {
  miriam-gene:2566 a ncit:C16612 .
  lld:C0014548 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_provenance {
  dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_assertion dcterms:description "[Our linkage analyses in 63 families ascertained through IGE patients with either juvenile myoclonic epilepsy, juvenile absence epilepsy or childhood absence epilepsy do not support the hypothesis that variants within the GABRA1 and GABRG2 gene cluster contribute a frequent major gene effect to the expression of the common familial IGEs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP761632.RAo4JIHBConBqyoOHa-b2ovdxowmqa9zCYJALZRfkk-vQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:41+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
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}