@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk> .
@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:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_head {
  this: np:hasAssertion dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_assertion;
    np:hasProvenance dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_provenance;
    np:hasPublicationInfo dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_assertion a np:Assertion .
  
  dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_provenance a np:Provenance .
  
  dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_assertion {
  miriam-gene:4988 a ncit:C16612 .
  
  lld:C0038580 a ncit:C7057 .
  
  dgn-gda:DGNa8abf574e37a7c43832e2fe8e813967c sio:SIO_000628 miriam-gene:4988, lld:C0038580;
    a sio:SIO_001122 .
}

dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_provenance {
  dgn-np:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_assertion dcterms:description
      "[Additional research is needed to determine whether these findings reflect no role for OPRM1 in determining risk for SD or whether another polymorphism in the gene influences receptor function and risk for SD.]. 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:16387451;
    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:NP53453.RAxzzoy8Cc2ZqoCrLeIyp4sCyTnhB929-YBC2NcTDKgNk130_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" .
}