sub:provenance {
  sub:assertion dcterms:description "[The aim of our study was to investigate novel mutations of Eph genes (EPHA1-8, EPHB1-4, EPHB6) and their association with clinically relevant mutations in BRAF, EML4-ALK, EGFR, INSR, KDR, KRAS, MET, PDGFRA, PDGFRB, PIK3, PTEN, RET, and TP53 in NSCLC 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:24123310 ;
    
prov:wasDerivedFrom dgn-void:BEFREE ;
    
prov:wasGeneratedBy eco:ECO_0000203 . 
  
dgn-void:BEFREE pav:importedOn "2017-02-19"^^
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 . 
}