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- NCIT_C84952 IAO_0000115 "Human HBB wt allele is located in the vicinity of 11p15.5 and is approximately 4 kb in length. This allele, which encodes hemoglobin subunit beta protein, plays a role in the transport of oxygen to tissues of the body. Mutations in this gene are associated with beta-thalassemia." @default.
- NCIT_C84952 NCIT_NHC0 "C84952" @default.
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- NCIT_C84952 NCIT_P106 "Gene or Genome" @default.
- NCIT_C84952 NCIT_P107 "HBB wt Allele" @default.
- NCIT_C84952 NCIT_P108 "HBB wt Allele" @default.
- NCIT_C84952 NCIT_P207 "C2827561" @default.
- NCIT_C84952 NCIT_P321 "3043" @default.
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- NCIT_C84952 normalizedInformationContent "100" @default.
- NCIT_C84952 referenceCount "1" @default.
- NCIT_C84952 hasExactSynonym "B-Globin Gene" @default.
- NCIT_C84952 hasExactSynonym "Beta-Globin Gene" @default.
- NCIT_C84952 hasExactSynonym "CD113t-C" @default.
- NCIT_C84952 hasExactSynonym "ECYT6" @default.
- NCIT_C84952 hasExactSynonym "HBB wt Allele" @default.
- NCIT_C84952 hasExactSynonym "Hemoglobin Beta wt Allele" @default.
- NCIT_C84952 hasExactSynonym "Hemoglobin, Beta Gene" @default.
- NCIT_C84952 hasExactSynonym "Hemoglobin--Beta Locus" @default.
- NCIT_C84952 hasExactSynonym "Hemoglobin-Beta Locus" @default.
- NCIT_C84952 inSubset NCIT_C116977 @default.
- NCIT_C84952 inSubset NCIT_C142799 @default.
- NCIT_C84952 inSubset NCIT_C142800 @default.
- NCIT_C84952 type Class @default.
- NCIT_C84952 isDefinedBy ncit.owl @default.
- NCIT_C84952 label "HBB wt Allele" @default.
- NCIT_C84952 subClassOf B644dba365acdf5c476137253a28e47f2 @default.
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