@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI> .
@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:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_head {
  this: np:hasAssertion dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_assertion;
    np:hasProvenance dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_provenance;
    np:hasPublicationInfo dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_assertion a np:Assertion .
  
  dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_provenance a np:Provenance .
  
  dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_assertion {
  miriam-gene:2562 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
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dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_provenance {
  dgn-np:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_assertion dcterms:description
      "[We conclude that  GABRA4 is involved in the etiology of autism and potentially increases autism risk through interaction with GABRB1. These results support the hypothesis that GABA receptor subunit genes are involved in autism, most likely via complex gene-gene interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:16080114;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP43730.RA5gh17PpOOqm3haZWg8pUAs0_RaQkiU712wQ2YGIXLeI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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