@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I> .
@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:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_head {
  this: np:hasAssertion dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion;
    np:hasProvenance dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_provenance;
    np:hasPublicationInfo dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion a np:Assertion .
  
  dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_provenance a np:Provenance .
  
  dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion {
  miriam-gene:4128 a ncit:C16612 .
  
  lld:C0019337 a ncit:C7057 .
  
  dgn-gda:DGNb457b5016da7f03a73aa034efc728719 sio:SIO_000628 miriam-gene:4128, lld:C0019337;
    a sio:SIO_001122 .
}

dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_provenance {
  dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion dcterms:description
      "[The long-repeat allelic variants (>4-repeats) and 2-repeat allele of the DRD4 exon 3 VNTR polymorphism might be risk alleles for individual vulnerability to heroin addiction in Chinese men, but the MAOA promoter VNTR polymorphism does not mean that the partial dominant inherited mode might involved in the genetics of 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:20218801;
    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:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}