@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_head {
  this: np:hasAssertion dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_assertion ;
    np:hasProvenance dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_provenance ;
    np:hasPublicationInfo dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_assertion a np:Assertion .
  dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_provenance a np:Provenance .
  dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_assertion {
  miriam-gene:1138 a ncit:C16612 .
  lld:C0242379 a ncit:C7057 .
  dgn-gda:DGNe841ef725dcf9741718e42cd9ca292db sio:SIO_000628 miriam-gene:1138 , lld:C0242379 ;
    a sio:SIO_001121 .
}
dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_provenance {
  dgn-np:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_assertion dcterms:description "[These findings suggest that SNPs in the CHRNA3 and CHRNA5 region contribute to lung cancer risk, and while variant alleles are less frequent in African Americans, risk in this group may be greater than in whites and less likely to reflect an indirect effect on lung cancer risk through nicotine dependence.]. 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:19641473 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP754309.RA7cje-EdRXHlDVBlQReytXbDcRED2EY3oWWp49wxs_so130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:27+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}