@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0> .
@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:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_head {
  this: np:hasAssertion dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_assertion;
    np:hasProvenance dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_provenance;
    np:hasPublicationInfo dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_assertion a np:Assertion .
  
  dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_provenance a np:Provenance .
  
  dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C0152115 a ncit:C7057 .
  
  dgn-gda:DGN4432bcf9f16f0b457f3679133041f246 sio:SIO_000628 miriam-gene:1813, lld:C0152115;
    a sio:SIO_001122 .
}

dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_provenance {
  dgn-np:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_assertion dcterms:description
      "[To further investigate whether the functional polymorphisms of dopamine D2 receptor (DRD2) and dopamine D3 receptor (DRD3) genes associate with the development of tardive dyskinesia (TD) in schizophrenia, and whether the interactive effects of DRD2, DRD3, 5-hydroxytryptamine 2C receptor (HTR2C) and manganese superoxide dismutase (MnSOD) genes contribute to the severity of TD.]. 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:12673575;
    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:NP45429.RAT3ijIjsGQH5XhPbIQpO_DfkKc2sHfChCVhS2id42He0130_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" .
}