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- NCIT_C124876 IAO_0000115 "Human HFE wild-type allele is located in the vicinity of 6p21.3 and is approximately 11 kb in length. This allele, which encodes hereditary hemochromatosis protein, is involved in iron homeostasis. Mutation of the gene is associated with hemochromatosis and microvascular complications of diabetes 7." @default.
- NCIT_C124876 NCIT_NHC0 "C124876" @default.
- NCIT_C124876 NCIT_P100 "613609" @default.
- NCIT_C124876 NCIT_P102 "NM_001300749" @default.
- NCIT_C124876 NCIT_P106 "Gene or Genome" @default.
- NCIT_C124876 NCIT_P108 "HFE wt Allele" @default.
- NCIT_C124876 NCIT_P207 "C4085201" @default.
- NCIT_C124876 NCIT_P321 "3077" @default.
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- NCIT_C124876 normalizedInformationContent "100" @default.
- NCIT_C124876 referenceCount "1" @default.
- NCIT_C124876 hasExactSynonym "HFE wt Allele" @default.
- NCIT_C124876 hasExactSynonym "HFE1" @default.
- NCIT_C124876 hasExactSynonym "HH" @default.
- NCIT_C124876 hasExactSynonym "HLA-H" @default.
- NCIT_C124876 hasExactSynonym "HLAH" @default.
- NCIT_C124876 hasExactSynonym "Hemochromatosis wt Allele" @default.
- NCIT_C124876 hasExactSynonym "High Fe Gene" @default.
- NCIT_C124876 hasExactSynonym "MVCD7" @default.
- NCIT_C124876 hasExactSynonym "TFQTL2" @default.
- NCIT_C124876 type Class @default.
- NCIT_C124876 isDefinedBy ncit.owl @default.
- NCIT_C124876 label "HFE wt Allele" @default.
- NCIT_C124876 subClassOf B37ffc50d85b0df8ecf7fe0aa599e73fd @default.
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- NCIT_C124876 subClassOf NCIT_C124875 @default.
- NCIT_C124876 subClassOf NCIT_C124876 @default.
- NCIT_C124876 subClassOf NCIT_C16612 @default.
- NCIT_C124876 subClassOf NCIT_C20194 @default.