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- B2c25a8654822369cba2bffa1e17a90e9 NCIT_P378 "NCI" @default.
- B2c25a8654822369cba2bffa1e17a90e9 type Axiom @default.
- B2c25a8654822369cba2bffa1e17a90e9 annotatedProperty IAO_0000115 @default.
- B2c25a8654822369cba2bffa1e17a90e9 annotatedSource NCIT_C84956 @default.
- B2c25a8654822369cba2bffa1e17a90e9 annotatedTarget "Human HBG1 wt allele is located in the vicinity of 11p15.5 and is approximately 2 kb in length. This allele, which encodes hemoglobin subunit gamma-1 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.