@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_head {
  this: np:hasAssertion dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_assertion;
    np:hasProvenance dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_provenance;
    np:hasPublicationInfo dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_assertion a np:Assertion .
  
  dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_provenance a np:Provenance .
  
  dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_assertion {
  miriam-gene:1815 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGN47745f0033e91207e1d55a2e1fc7820f sio:SIO_000628 miriam-gene:1815, lld:C0525045;
    a sio:SIO_001121 .
}

dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_provenance {
  dgn-np:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_assertion dcterms:description
      "[Future studies that include the sequence variants within the 48 bp motif of the DRD4 coding region polymorphism, and possibly alternate definitions of the affective disorder phenotype, may provide more definitive answers.]. 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:7914460;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1326574.RAjlC6DdKdEk30Q7GclnXlueOQ0Ch0ClbNkRjvUKTn6cw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:47+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}