dgn-np:NP1266171.RAzfYuyRhXbNCkN1eK8_vZNQ5IFg25sYpU_OkrkcZcy7Q130_provenance {
  dgn-np:NP1266171.RAzfYuyRhXbNCkN1eK8_vZNQ5IFg25sYpU_OkrkcZcy7Q130_assertion dcterms:description "[It has become apparent that there are very few highly recurrently mutated genes such as TP53, PIK3CA, and GATA3, that no two breast cancers display an identical repertoire of somatic genetic alterations at base-pair resolution and that there might not be a single highly recurrently mutated gene that defines each of the intrinsic subtypes of breast cancer (ie, basal-like, HER2-enriched, luminal A, and luminal B).]. 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:25713166 ;
    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 .
}