@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY> .
@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:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_head {
  this: np:hasAssertion dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_assertion ;
    np:hasProvenance dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_provenance ;
    np:hasPublicationInfo dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_assertion a np:Assertion .
  dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_provenance a np:Provenance .
  dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_assertion {
  miriam-gene:2950 a ncit:C16612 .
  lld:C0001418 a ncit:C7057 .
  dgn-gda:DGNa93bdbff50494c173fd0ce1d3f7a5e35 sio:SIO_000628 miriam-gene:2950 , lld:C0001418 ;
    a sio:SIO_001121 .
}
dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_provenance {
  dgn-np:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_assertion dcterms:description "[In presented case-control study we investigate the incidence of polymorphism of GSTT1, GSTM1, GSTP1 genes and their combinations as possible predictive factors for identification of individuals with increased risk of formation and development of adenocarcinoma (AC) and squamous cell carcinoma (SCC) of lung in Slovak population.]. 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:22248273 ;
    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:NP588985.RA8aPoHUpGKGVFFf2zeXhm9sb0MXKP7H1E9b2iuT_xkqY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+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> ;
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    pav:version "v2.1.0.0" .
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}