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- NCIT_C188389 IAO_0000115 "Human APOE*2 allele is located in the vicinity of 19q13.2 and is approximately 4 kb in length. This allele, which encodes apolipoprotein E2 protein, plays a role in lipid transport and triglyceride metabolism. The allele is associated with type III hyperlipoproteinemia." @default.
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- NCIT_C188389 NCIT_P106 "Gene or Genome" @default.
- NCIT_C188389 NCIT_P107 "APOE*2 Allele" @default.
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- NCIT_C188389 NCIT_P98 "APOE*2 allele is characterized by one point mutation, c.526C>T. The ancestral thymine at position 388 must also be present." @default.
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- NCIT_C188389 hasExactSynonym "APOE*2 Allele" @default.
- NCIT_C188389 hasExactSynonym "APOE*E2" @default.
- NCIT_C188389 hasExactSynonym "APOE-epsilon2 Allele" @default.
- NCIT_C188389 hasExactSynonym "APOE2 Allele" @default.
- NCIT_C188389 hasExactSynonym "ApoE2" @default.
- NCIT_C188389 hasExactSynonym "Apolipoprotein E*2 Allele" @default.
- NCIT_C188389 hasExactSynonym "Apolipoprotein E2 Allele" @default.
- NCIT_C188389 hasExactSynonym "NM_000041.4:c.526C>T" @default.
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- NCIT_C188389 label "APOE*2 Allele" @default.
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