@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw> .
@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:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_head {
  this: np:hasAssertion dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_assertion ;
    np:hasProvenance dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_provenance ;
    np:hasPublicationInfo dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  lld:C0007130 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_provenance {
  dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_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 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP756390.RA-OABeOD7ZgkDZP1LqxqD1hsWIXjDfRTs0LFaSlkVQCw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:38+02:00"^^xsd:dateTime ;
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    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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