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- NCIT_C126957 IAO_0000115 "Human C2 wild-type allele is located in the vicinity of 6p21.3 and is approximately 48 kb in length. This allele, which encodes complement C2 protein, plays a role in proteolysis and complement activation. Mutation of the gene is associated with C2 deficiency and increased susceptibility for age-related macular degeneration." @default.
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- NCIT_C126957 NCIT_P106 "Gene or Genome" @default.
- NCIT_C126957 NCIT_P107 "C2 wt Allele" @default.
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- NCIT_C126957 hasExactSynonym "ARMD14" @default.
- NCIT_C126957 hasExactSynonym "C2 wt Allele" @default.
- NCIT_C126957 hasExactSynonym "CO2" @default.
- NCIT_C126957 hasExactSynonym "Complement Component 2 wt Allele" @default.
- NCIT_C126957 inSubset NCIT_C116977 @default.
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- NCIT_C126957 type Class @default.
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- NCIT_C126957 label "C2 wt Allele" @default.
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