@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4> .
@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:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_head {
  this: np:hasAssertion dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_assertion;
    np:hasProvenance dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_provenance;
    np:hasPublicationInfo dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_assertion a np:Assertion .
  
  dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_provenance a np:Provenance .
  
  dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_assertion {
  miriam-gene:2947 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN75868fea97311f69e70e8522a67e69f4 sio:SIO_000628 miriam-gene:2947, lld:C0242379;
    a sio:SIO_001122 .
}

dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_provenance {
  dgn-np:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_assertion dct:description
      "[Based on the literature, the alleles of the genotypes were categorised as high- or low-risk alleles. No individual effect of the genotypes was found on the risk of lung cancer. Given a smoking exposure, the presence of high-risk alleles (or phenotypes) was generally found to increase the risk of lung cancer, although the effect modification did not reach statistical significance. A pattern of stronger protective effect was observed in carriers of more than one allele associated with lower risk of lung cancer, and a higher risk of lung cancer in carriers of one or more alleles associated with higher risk of lung cancer, but the results did not reach statistical significance. The effect modification was generally strongest at lower levels of smoking.]. 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:15829318;
    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:NP43061.RAvlWZZpSaKQe_Rz_iRdOJN5kCKBRQu_1ByMz9mxh1Me4130_publicationInfo {
  this: dct:created "2014-10-02T12:32:19+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" .
}