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- NCIT_C189198 IAO_0000115 "Human APOA2 wild-type allele is located in the vicinity of 1q23.3 and is approximately 1 kb in length. This allele, which encodes apolipoprotein A-II protein, plays a role in high density lipoprotein-dependent cholesterol transport and metabolism. Mutation of the gene is associated with apolipoprotein A-II deficiency or hypercholesterolemia." @default.
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- NCIT_C189198 NCIT_P102 "NM_001643" @default.
- NCIT_C189198 NCIT_P106 "Gene or Genome" @default.
- NCIT_C189198 NCIT_P108 "APOA2 wt Allele" @default.
- NCIT_C189198 NCIT_P208 "CL1794166" @default.
- NCIT_C189198 NCIT_P321 "336" @default.
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- NCIT_C189198 hasExactSynonym "APOA2 wt Allele" @default.
- NCIT_C189198 hasExactSynonym "Apo-AII" @default.
- NCIT_C189198 hasExactSynonym "ApoA-II" @default.
- NCIT_C189198 hasExactSynonym "ApoAII" @default.
- NCIT_C189198 hasExactSynonym "Apolipoprotein A2 wt Allele" @default.
- NCIT_C189198 type Class @default.
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- NCIT_C189198 label "APOA2 wt Allele" @default.
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