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- NCIT_C116409 IAO_0000115 "Human ABCA1 wild-type allele is located in the vicinity of 9q31 and is approximately 147 kb in length. This allele, which encodes ATP-binding cassette sub-family A member 1 protein, is involved in intracellular cholesterol transport. Mutation of the gene is associated with high density lipoprotein deficiency type 2 (autosomal dominant) and Tangier disease." @default.
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- NCIT_C116409 NCIT_P106 "Gene or Genome" @default.
- NCIT_C116409 NCIT_P107 "ABCA1 wt Allele" @default.
- NCIT_C116409 NCIT_P108 "ABCA1 wt Allele" @default.
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- NCIT_C116409 hasExactSynonym "ABC-1" @default.
- NCIT_C116409 hasExactSynonym "ABC1" @default.
- NCIT_C116409 hasExactSynonym "ABCA1 wt Allele" @default.
- NCIT_C116409 hasExactSynonym "ATP-Binding Cassette, Sub-Family A (ABC1), Member 1 wt Allele" @default.
- NCIT_C116409 hasExactSynonym "ATP-Binding Cassette, Subfamily A, Member 1 Gene" @default.
- NCIT_C116409 hasExactSynonym "CERP" @default.
- NCIT_C116409 hasExactSynonym "HDLDT1" @default.
- NCIT_C116409 hasExactSynonym "TGD" @default.
- NCIT_C116409 hasExactSynonym "Tangier Disease Gene" @default.
- NCIT_C116409 inSubset NCIT_C116977 @default.
- NCIT_C116409 inSubset NCIT_C142799 @default.
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- NCIT_C116409 type Class @default.
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