@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA> .
@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:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_head {
  this: np:hasAssertion dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_assertion;
    np:hasProvenance dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_provenance;
    np:hasPublicationInfo dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_assertion a np:Assertion .
  
  dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_provenance a np:Provenance .
  
  dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0699893 a ncit:C7057 .
  
  dgn-gda:DGN684476a3412c2d424744aaed4bd50e75 sio:SIO_000628 miriam-gene:2944, lld:C0699893;
    a sio:SIO_001121 .
}

dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_provenance {
  dgn-np:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_assertion dcterms:description
      "[Analysis of allelism and interaction between allelic variants showed significant association between combined GSTM1 and CYP1A1 Val(462) genotypes, where individuals homozygous for the risk allele GSTM1 null and carrying also the allele CYP1A1 Val(462), show a higher risk of developing NMSC [OR 4.5 (1.1-21.4); P = 0.03], especially SCC [OR 6.5 (1.4-34.4); P = 0.01].]. 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:17083362;
    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:NP185470.RA4vBATVKzIy8vvelUZf-kedPdgybdymikuSzWfZcjRIA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:42+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" .
}