@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q> .
@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:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_head {
  this: np:hasAssertion dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_assertion;
    np:hasProvenance dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_provenance;
    np:hasPublicationInfo dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_assertion a np:Assertion .
  
  dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_provenance a np:Provenance .
  
  dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C0152115 a ncit:C7057 .
  
  dgn-gda:DGNca2414059866bc2c74f50215408c35ec sio:SIO_000628 miriam-gene:1813, lld:C0152115;
    a sio:SIO_001122 .
}

dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_provenance {
  dgn-np:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_assertion dcterms:description
      "[We examined three polymorphisms in the dopamine D2 receptor gene (DRD2), two sites in the 3' region of the dopamine transporter (DAT) gene, two sites in the promoter and coding region of the dopamine D4 (DRD4) receptor gene, as well as polymorphic sites in the serotonin 6 receptor gene, the serotonin transporter gene and the tryptophan hydroxylase gene, for association with TD susceptibility.]. 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:NP45430.RAVwZATzgLY2-6ST60oZ7DmTqtOgJ4ErQhby_rHUtHU9Q130_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>,
      <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" .
}