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- B7e9d256eafc56dd9a27b8a8d081f3f2d NCIT_P378 "NCI" @default.
- B7e9d256eafc56dd9a27b8a8d081f3f2d type Axiom @default.
- B7e9d256eafc56dd9a27b8a8d081f3f2d annotatedProperty IAO_0000115 @default.
- B7e9d256eafc56dd9a27b8a8d081f3f2d annotatedSource NCIT_C84959 @default.
- B7e9d256eafc56dd9a27b8a8d081f3f2d annotatedTarget "Human HBG2 wt allele is located in the vicinity of 11p15.5 and is approximately 393 kb in length. This allele, which encodes hemoglobin subunit gamma-2 protein, plays a role in the transport of oxygen to tissues of the fetal and neonatal body. Mutations in this gene may be associated with beta-thalassemia." @default.