@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8> .
@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 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:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_head {
  this: np:hasAssertion dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_assertion;
    np:hasProvenance dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_provenance;
    np:hasPublicationInfo dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_assertion a np:Assertion .
  
  dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_provenance a np:Provenance .
  
  dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_assertion {
  miriam-gene:284217 a ncit:C16612 .
  
  lld:C0040336 a ncit:C7057 .
  
  dgn-gda:DGNd26fb4bd09d2eff0409afd63abbb47c5 sio:SIO_000628 miriam-gene:284217, lld:C0040336;
    a sio:SIO_001122 .
}

dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_provenance {
  dgn-np:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_assertion dct:description
      "[These results support polygenic genetics for success in abstaining from smoking, overlap with genetics of substance dependence and memory, and nominate gene variants for selective influences on therapeutic responses to bupropion vs NRT.]. 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:18519826;
    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:NP71036.RAVCo1aOIEzPWap4gwbMLS13hF8DBTL75df0LrlchIj_8130_publicationInfo {
  this: dct:created "2014-10-02T12:32:34+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}