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- Bca3f4f9fe12f391d879277f3c5bc02e0 NCIT_P378 "NCI" @default.
- Bca3f4f9fe12f391d879277f3c5bc02e0 type Axiom @default.
- Bca3f4f9fe12f391d879277f3c5bc02e0 annotatedProperty IAO_0000115 @default.
- Bca3f4f9fe12f391d879277f3c5bc02e0 annotatedSource NCIT_C97321 @default.
- Bca3f4f9fe12f391d879277f3c5bc02e0 annotatedTarget "Human ASXL1 wild-type allele is located in the vicinity of 20q11 and is approximately 81 kb in length. This allele, which encodes putative Polycomb group protein ASXL1, may play a role in the regulation of both chromatin structure and transcription. Mutation of the gene is associated with both myelodysplastic syndromes and chronic myelomonocytic leukemia." @default.