@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4> .
@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:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_head {
  this: np:hasAssertion dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion;
    np:hasProvenance dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_provenance;
    np:hasPublicationInfo dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion a np:Assertion .
  
  dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_provenance a np:Provenance .
  
  dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion {
  miriam-gene:4780 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN5affc0b935f47371f6e247c6bd6edd58 sio:SIO_000628 miriam-gene:4780, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_provenance {
  dgn-np:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_assertion dcterms:description
      "[In excellent agreement with this finding, we found that minor A/A homozygotes of a single nucleotide polymorphism (SNP) in the human NRF2 upstream promoter region (rs6721961) exhibited significantly diminished NRF2 gene expression and, consequently, an increased risk of lung cancer, especially those who had ever smoked.]. 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:23572560;
    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:NP799133.RAmG-TrXK4xZoR1WI4QpG467RB8Zp29T5AWxml448NZc4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:10+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" .
}