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- NCIT_C84956 IAO_0000115 "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.
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- NCIT_C84956 NCIT_P106 "Gene or Genome" @default.
- NCIT_C84956 NCIT_P107 "HBG1 wt Allele" @default.
- NCIT_C84956 NCIT_P108 "HBG1 wt Allele" @default.
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- NCIT_C84956 normalizedInformationContent "100" @default.
- NCIT_C84956 referenceCount "1" @default.
- NCIT_C84956 hasExactSynonym "HBG1 wt Allele" @default.
- NCIT_C84956 hasExactSynonym "HBGA" @default.
- NCIT_C84956 hasExactSynonym "HBGR" @default.
- NCIT_C84956 hasExactSynonym "HSGGL1" @default.
- NCIT_C84956 hasExactSynonym "Hemoglobin Gamma A wt Allele" @default.
- NCIT_C84956 hasExactSynonym "PRO2979" @default.
- NCIT_C84956 inSubset NCIT_C116977 @default.
- NCIT_C84956 inSubset NCIT_C142799 @default.
- NCIT_C84956 inSubset NCIT_C142800 @default.
- NCIT_C84956 type Class @default.
- NCIT_C84956 isDefinedBy ncit.owl @default.
- NCIT_C84956 label "HBG1 wt Allele" @default.
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