@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI> .
@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:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_head {
  this: np:hasAssertion dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_assertion;
    np:hasProvenance dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_provenance;
    np:hasPublicationInfo dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_assertion a np:Assertion .
  
  dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_provenance a np:Provenance .
  
  dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_assertion {
  miriam-gene:1553 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN451d5059ca741df76d1e9aac4ee6e9f3 sio:SIO_000628 miriam-gene:1553, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_provenance {
  dgn-np:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_assertion dcterms:description
      "[In this case-control study, we genotyped 724 patients with lung cancer and 791 controls for this polymorphism to examine the hypothesis that the variant CYP2A13 may have impact on risk of lung cancer in relation to tobacco 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:14633739;
    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:NP667182.RAZecGq1BZx2TXjTTFtGOvrfacgWphkqhYxqcLRrnsiSI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:43+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" .
}