@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA> .
@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:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_head {
  this: np:hasAssertion dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_assertion;
    np:hasProvenance dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_provenance;
    np:hasPublicationInfo dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_assertion a np:Assertion .
  
  dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_provenance a np:Provenance .
  
  dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_assertion {
  miriam-gene:9904 a ncit:C16612 .
  
  lld:C0040336 a ncit:C7057 .
  
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    a sio:SIO_001122 .
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dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_provenance {
  dgn-np:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_assertion dcterms: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:NP75912.RAmlXqO1fmc-LNk6in76mv9s2iJTHP9vgviHI5Sb2OkSA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:37+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}