@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94> .
@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:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_head {
  this: np:hasAssertion dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_assertion;
    np:hasProvenance dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_provenance;
    np:hasPublicationInfo dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_assertion a np:Assertion .
  
  dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_provenance a np:Provenance .
  
  dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGN8bfcf75c37ce8926db6c89fb62a24a7c sio:SIO_000628 miriam-gene:3845, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_provenance {
  dgn-np:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_assertion dcterms:description
      "[These results suggest that mutations are good markers of different aetiologies and histopathological forms of lung cancers but have little prognostic value, with the exception of KRAS mutation, which may have a prognostic value in ADC.]. 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:22267755;
    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:NP265053.RACecK9jKuEXrk8Ko8TVJ8XEjHIgevlKVZE1DRFUJqd94130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}