@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g> .
@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:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_head {
  this: np:hasAssertion dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion;
    np:hasProvenance dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_provenance;
    np:hasPublicationInfo dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion a np:Assertion .
  
  dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_provenance a np:Provenance .
  
  dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion {
  miriam-gene:4810 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNab0ce61ad3f3faffa4a8a0e4cf3d6357 sio:SIO_000628 miriam-gene:4810, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_provenance {
  dgn-np:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_assertion dcterms:description
      "[The contribution of common genetic variation to one or more established smoking behaviors was investigated in a joint analysis of two genome wide association studies (GWAS) performed as part of the Cancer Genetic Markers of Susceptibility (CGEMS) project in 2,329 men from the Prostate, Lung, Colon and Ovarian (PLCO) Trial, and 2,282 women from the Nurses' Health Study (NHS).]. 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:19247474;
    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:NP482127.RAfeVRSN22IDE4icP-g1r1WWm5Kim_LZgAtZiV9bTjZ4g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:48+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" .
}