@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc> .
@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:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_head {
  this: np:hasAssertion dgn-np:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_assertion;
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    np:hasPublicationInfo dgn-np:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_publicationInfo a
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}

dgn-np:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_assertion {
  miriam-gene:6531 a ncit:C16612 .
  
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dgn-np:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_provenance {
  dgn-np:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_assertion dcterms:description
      "[For the first time, these findings provide tentative evidence of the contribution of the DAT1 gene core promoter polymorphism to the etiopathophysiology of bipolar disorder at least in the Iranian population that we have studied. Interestingly, no allelic or genotype association was observed in the female patients (P]. 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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  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:NP51582.RAgHxNGsHeXXcFt8AUCdsWystWyTDcPP6ow7z-cRIPwcc130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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