@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY> .
@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:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_head {
  this: np:hasAssertion dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion;
    np:hasProvenance dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_provenance;
    np:hasPublicationInfo dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion a np:Assertion .
  
  dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_provenance a np:Provenance .
  
  dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion {
  miriam-gene:10923 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGNc356820df7e5d272d1c58bec34214094 sio:SIO_000628 miriam-gene:10923, lld:C0007131;
    a sio:SIO_001121 .
}

dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_provenance {
  dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion dcterms:description
      "[We have analyzed EGFR and HER2 mutations and the expression of the two products of the CDKN2A gene (p14(arf) and p16(INK4a)) in 116 NSCLC that have been previously analyzed for TP53 and KRAS mutations in relation to smoking history of patients.]. 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:17575133;
    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:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}