@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE> .
@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:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_head {
  this: np:hasAssertion dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_assertion;
    np:hasProvenance dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_provenance;
    np:hasPublicationInfo dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_assertion a np:Assertion .
  
  dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_provenance a np:Provenance .
  
  dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_assertion {
  miriam-gene:2064 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGN26ce6904ab6d250a3d817770c3df2271 sio:SIO_000628 miriam-gene:2064, lld:C0007131;
    a sio:SIO_001121 .
}

dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_provenance {
  dgn-np:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_assertion dcterms:description
      "[We analyzed the mutational status of exons 9 and 20 and gene copy number of PIK3CA using 86 non-small cell lung cancer (NSCLC) cell lines, 43 small cell lung cancer (SCLC) cell lines, 3 extrapulmonary small cell cancer (ExPuSC) cell lines, and 691 resected NSCLC tumors and studied the relationship between PIK3CA alterations and mutational status of epidermal growth factor receptor (EGFR) signaling pathway genes (EGFR, KRAS, HER2, and BRAF).]. 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:18757405;
    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:NP167597.RAUms_GFV9xJ2ISmlZ2UgjgNoch-kaXmLxhKfqhXnJgDE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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>;
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