@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE> .
@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:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_head {
  this: np:hasAssertion dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_assertion;
    np:hasProvenance dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_provenance;
    np:hasPublicationInfo dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_assertion a np:Assertion .
  
  dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_provenance a np:Provenance .
  
  dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_assertion {
  miriam-gene:3358 a ncit:C16612 .
  
  lld:C0686347 a ncit:C7057 .
  
  dgn-gda:DGN0e01a81d2576904fe949d3399b9ec05e sio:SIO_000628 miriam-gene:3358, lld:C0686347;
    a sio:SIO_001121 .
}

dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_provenance {
  dgn-np:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_assertion dcterms:description
      "[The primary focus has been on SNPs in dopamine and serotonin receptor genes: persuasive meta-analytic evidence exists for an effect of the dopamine D2 and D3 receptor genes (DRD2 and DRD3) in risk for tardive dyskinesia (TD) and for an effect of variation at the 5-HT2C receptor gene (HTR2C) for liability to APD-induced weight gain.]. 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:20135898;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP769743.RAGtidwVhCBkMBdftROZY4RlXa_7jyBbHhTNB0H-xYHGE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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>,
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
}