@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ> .
@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:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_head {
  this: np:hasAssertion dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion;
    np:hasProvenance dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance;
    np:hasPublicationInfo dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion a np:Assertion .
  
  dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance a np:Provenance .
  
  dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion {
  miriam-gene:7166 a ncit:C16612 .
  
  lld:C0152115 a ncit:C7057 .
  
  dgn-gda:DGNbd57012b9864230d847c88d9cae1dd79 sio:SIO_000628 miriam-gene:7166, lld:C0152115;
    a sio:SIO_001122 .
}

dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_provenance {
  dgn-np:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_assertion dcterms:description
      "[No significant associations were found. Within the limitations imposed by the size of the clinical sample, these findings suggest that the above polymorphic loci do not contribute significantly to risk for TD. Further examination of loci that yielded positive results at a trend level and investigation of other candidate genetic loci coding for antipsychotic drug targets is warranted.]. 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:14583797;
    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:NP58804.RAaj5UQXcRCrvQIbEZMxQDbv-B0cC3SDEPOf0I_TwEOzQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}