@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4> .
@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:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_head {
  this: np:hasAssertion dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_assertion;
    np:hasProvenance dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_provenance;
    np:hasPublicationInfo dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_assertion a np:Assertion .
  
  dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_provenance a np:Provenance .
  
  dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_assertion {
  miriam-gene:1815 a ncit:C16612 .
  
  lld:C1263846 a ncit:C7057 .
  
  dgn-gda:DGNcaebcfc628864424514810e6149f48d6 sio:SIO_000628 miriam-gene:1815, lld:C1263846;
    a sio:SIO_001122 .
}

dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_provenance {
  dgn-np:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_assertion dcterms:description
      "[There was no significant association between dopamine D4 receptor gene alleles, Novelty Seeking traits, and the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition diagnosis of attention deficit hyperactivity disorder--Hyperactive impulsive type or Inattentive type.]. 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:15519116;
    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:NP45323.RAz448RH1Xeh8VeEXO96N8OvZdtFYhXVOw-sZ9usXpxn4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}