@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8> .
@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 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:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_head {
  this: np:hasAssertion dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion;
    np:hasProvenance dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_provenance;
    np:hasPublicationInfo dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion a np:Assertion .
  
  dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_provenance a np:Provenance .
  
  dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion {
  miriam-gene:2555 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
  dgn-gda:DGN11e33ae0ce4c6c2b4b1926f1071b426a sio:SIO_000628 miriam-gene:2555, lld:C0004352;
    a sio:SIO_001122 .
}

dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_provenance {
  dgn-np:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_assertion dct: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:NP43774.RAgDrCap96LY7aOJoDZ7X3JUadYszCEhQU189mo2PyyZ8130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}