@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA> .
@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:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_head {
  this: np:hasAssertion dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_assertion;
    np:hasProvenance dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_provenance;
    np:hasPublicationInfo dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_assertion a np:Assertion .
  
  dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_provenance a np:Provenance .
  
  dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C0003431 a ncit:C7057 .
  
  dgn-gda:DGN73ff716b4ceca8c30c06b1e939ef2bfb sio:SIO_000628 miriam-gene:1813, lld:C0003431;
    a sio:SIO_001121 .
}

dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_provenance {
  dgn-np:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_assertion dcterms:description
      "[The dopamine D2 (DRD2) gene, and especially its allele TaqI A1 allele and its receptor, also may be involved in comorbid antisocial personality disorder symptoms, high novelty seeking, and related traits.]. 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:15457501;
    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:NP187646.RAQhXPv6mv8k3v-hTWeUSaEqigD0Ad6GBJUQihPbtf0xA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}