@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg> .
@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:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_head {
  this: np:hasAssertion dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_assertion;
    np:hasProvenance dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_provenance;
    np:hasPublicationInfo dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_assertion a np:Assertion .
  
  dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_provenance a np:Provenance .
  
  dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_assertion {
  miriam-gene:1815 a ncit:C16612 .
  
  lld:C0030662 a ncit:C7057 .
  
  dgn-gda:DGN02750b5d6d5ce65ed4c6380d35e7405b sio:SIO_000628 miriam-gene:1815, lld:C0030662;
    a sio:SIO_001121 .
}

dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_provenance {
  dgn-np:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_assertion dcterms:description
      "[Prior studies have reported an association between the presence of the 7 repeat allele of the 48 bp repeat polymorphism of the third cytoplasmic loop of the dopamine D4 receptor gene (DRD4) and novelty seeking behaviors, attention deficit hyperactivity disorder (ADHD), Tourette syndrome (TS), pathological gambling, and substance abuse.]. 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:10402503;
    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:NP517085.RAJjNNzkyowveMXZOK6bX9CWDRN1zLsIxUVCCwpGr4obg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:08+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" .
}