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- NCIT_C178160 IAO_0000115 "Human C1S wild-type allele is located in the vicinity of 12p13.31 and is approximately 83 kb in length. This allele, which encodes complement C1s subcomponent protein, is involved in complement activation. Mutation of the gene is associated with Ehlers-Danlos syndrome periodontal type 2 and selective complement component C1s deficiency." @default.
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- NCIT_C178160 NCIT_P107 "C1S wt Allele" @default.
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- NCIT_C178160 hasExactSynonym "C1S wt Allele" @default.
- NCIT_C178160 hasExactSynonym "Complement C1s wt Allele" @default.
- NCIT_C178160 hasExactSynonym "Complement Component 1, S Subcomponent Gene" @default.
- NCIT_C178160 hasExactSynonym "EDSPD2" @default.
- NCIT_C178160 inSubset NCIT_C116977 @default.
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- NCIT_C178160 type Class @default.
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- NCIT_C178160 label "C1S wt Allele" @default.
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