@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc> .
@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:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_head {
  this: np:hasAssertion dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_assertion;
    np:hasProvenance dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_provenance;
    np:hasPublicationInfo dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_assertion a np:Assertion .
  
  dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_provenance a np:Provenance .
  
  dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_assertion {
  miriam-gene:6817 a ncit:C16612 .
  
  lld:C0024623 a ncit:C7057 .
  
  dgn-gda:DGN2a07888759fd14aeeb2c980c3c223582 sio:SIO_000628 miriam-gene:6817, lld:C0024623;
    a sio:SIO_001121 .
}

dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_provenance {
  dgn-np:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_assertion dcterms:description
      "[GSTT1, SULT1A1 and NAT2 polymorphisms appear to modulate individual's susceptibility to gastric cancer in this Italian population, particularly when more than one unfavourable genotype is present, or when combined with cigarette smoke.]. 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:17996038;
    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:NP273907.RAXelPWWPUoYCDQHcW2T8ET64OovozSn9vBmrIZDll-kc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:34+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" .
}