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- B1311afe76d1388509d26e3a009c7163a NCIT_P378 "NCI" @default.
- B1311afe76d1388509d26e3a009c7163a type Axiom @default.
- B1311afe76d1388509d26e3a009c7163a annotatedProperty IAO_0000115 @default.
- B1311afe76d1388509d26e3a009c7163a annotatedSource NCIT_C185939 @default.
- B1311afe76d1388509d26e3a009c7163a annotatedTarget "A molecular genetic abnormality indicating the presence of a deletion mutation in exon 19 of the EGFR gene that results in constitutive epidermal growth factor receptor-dependent signal transduction and activation of downstream signaling pathways." @default.