@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM> .
@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:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_head {
  this: np:hasAssertion dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion;
    np:hasProvenance dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_provenance;
    np:hasPublicationInfo dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion a np:Assertion .
  
  dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_provenance a np:Provenance .
  
  dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion {
  miriam-gene:6531 a ncit:C16612 .
  
  lld:C0019337 a ncit:C7057 .
  
  dgn-gda:DGN98c76637bcdb959b5e3e3d2563f19804 sio:SIO_000628 miriam-gene:6531, lld:C0019337;
    a sio:SIO_001121 .
}

dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_provenance {
  dgn-np:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_assertion dcterms:description
      "[Polymorphism of a variable number of tandem repeats (VNTR) in the 3' untranslated region of exon 15 of the SLC6A3 gene, coding for the dopamine transporter (DAT), was analysed to test whether length variation contributes to differences in the individual susceptibility to aggressive - criminal behaviour and liability to heroin dependence.]. 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:16109590;
    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:NP562668.RAKDGo4Uk8oW0yMeVJN_yTJVGLJMPlblSQLcB1uvYjZqM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:39+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" .
}