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- B8536e218bedc1c6da12cb52b935c0ab5 NCIT_P378 "NCI" @default.
- B8536e218bedc1c6da12cb52b935c0ab5 type Axiom @default.
- B8536e218bedc1c6da12cb52b935c0ab5 annotatedProperty IAO_0000115 @default.
- B8536e218bedc1c6da12cb52b935c0ab5 annotatedSource NCIT_C124874 @default.
- B8536e218bedc1c6da12cb52b935c0ab5 annotatedTarget "A cytogenetic abnormality that refers to the allelic gain of an internal part of chromosome 21. It is a rare high-risk chromosomal abnormality that occurs in approximately 2-5% of pediatric patients with B-cell precursor Acute Lymphoblastic Leukemia. This abnormality has been associated with a poor outcome in patients treated by standard protocols." @default.