@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM> .
@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:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_head {
  this: np:hasAssertion dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_assertion;
    np:hasProvenance dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_provenance;
    np:hasPublicationInfo dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_assertion a np:Assertion .
  
  dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_provenance a np:Provenance .
  
  dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0023532 a ncit:C7057 .
  
  dgn-gda:DGN63721224591d676e8616430917bfb4c9 sio:SIO_000628 miriam-gene:2952, lld:C0023532;
    a sio:SIO_001122 .
}

dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_provenance {
  dgn-np:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_assertion dcterms:description
      "[A positive association exists between the isolated or combined null genotype of GSTM1 and GSTT1 and oral leukoplakia development and the null GSTT1 genotype shows increased risk of p53 overexpression, in oral leukoplakia.]. 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:18507060;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP73906.RAVTvSAcCuw_A23UpFSKrcgRxSIIjK0HWIv_CFydBxEHM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}