@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_head {
  this: np:hasAssertion dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_assertion;
    np:hasProvenance dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_provenance;
    np:hasPublicationInfo dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_assertion a np:Assertion .
  
  dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_provenance a np:Provenance .
  
  dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_assertion {
  miriam-gene:10381 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGN3ae07215eec1fe640dc232b653428721 sio:SIO_000628 miriam-gene:10381, lld:C0007131;
    a sio:SIO_001121 .
}

dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_provenance {
  dgn-np:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_assertion dcterms:description
      "[NSCLC specimens that harboring EGFR-activating mutations are more likely to express low ERCC1 and high TUBB3 mRNA levels, whereas tumors from patients with NSCLC harboring KRAS mutation are more likely to express high ERCC1 mRNA levels.]. 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:24994038;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1198488.RAnGDpJn8yjXZQ9VO5yoVgMB_EMw4dPY_ruMGs0vbr-q0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:49+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}