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- NCIT_C84959 IAO_0000115 "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.
- NCIT_C84959 NCIT_NHC0 "C84959" @default.
- NCIT_C84959 NCIT_P100 "142250" @default.
- NCIT_C84959 NCIT_P102 "NM_000184" @default.
- NCIT_C84959 NCIT_P106 "Gene or Genome" @default.
- NCIT_C84959 NCIT_P107 "HBG2 wt Allele" @default.
- NCIT_C84959 NCIT_P108 "HBG2 wt Allele" @default.
- NCIT_C84959 NCIT_P207 "C2827564" @default.
- NCIT_C84959 NCIT_P321 "3048" @default.
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- NCIT_C84959 normalizedInformationContent "100" @default.
- NCIT_C84959 referenceCount "1" @default.
- NCIT_C84959 hasExactSynonym "FLJ76540" @default.
- NCIT_C84959 hasExactSynonym "HBG-T1" @default.
- NCIT_C84959 hasExactSynonym "HBG2 wt Allele" @default.
- NCIT_C84959 hasExactSynonym "Hemoglobin Gamma G Gene" @default.
- NCIT_C84959 hasExactSynonym "Hemoglobin Subunit Gamma 2 wt Allele" @default.
- NCIT_C84959 hasExactSynonym "Hemoglobin, Gamma G Gene" @default.
- NCIT_C84959 hasExactSynonym "Hemoglobin--Gamma Locus, 136 Glycine Gene" @default.
- NCIT_C84959 hasExactSynonym "TNCY" @default.
- NCIT_C84959 inSubset NCIT_C116977 @default.
- NCIT_C84959 inSubset NCIT_C142799 @default.
- NCIT_C84959 inSubset NCIT_C142800 @default.
- NCIT_C84959 type Class @default.
- NCIT_C84959 isDefinedBy ncit.owl @default.
- NCIT_C84959 label "HBG2 wt Allele" @default.
- NCIT_C84959 subClassOf B47351792a9380860fa5ace48946b8150 @default.
- NCIT_C84959 subClassOf B754557a6e82c9fe7908c5f0b12d8526c @default.
- NCIT_C84959 subClassOf NCIT_C142196 @default.
- NCIT_C84959 subClassOf NCIT_C16612 @default.
- NCIT_C84959 subClassOf NCIT_C21295 @default.
- NCIT_C84959 subClassOf NCIT_C28533 @default.
- NCIT_C84959 subClassOf NCIT_C84958 @default.
- NCIT_C84959 subClassOf NCIT_C84959 @default.