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- NCIT_C150252 IAO_0000115 "Human GSN wild-type allele is located in the vicinity of 9q33.2 and is approximately 125 kb in length. This allele, which encodes gelsolin protein, plays a role in both assembly and disassembly of actin filaments. Mutation of the gene is associated with Finnish type familial amyloidosis (amyloidosis V)." @default.
- NCIT_C150252 NCIT_NHC0 "C150252" @default.
- NCIT_C150252 NCIT_P100 "137350" @default.
- NCIT_C150252 NCIT_P102 "X04412" @default.
- NCIT_C150252 NCIT_P106 "Gene or Genome" @default.
- NCIT_C150252 NCIT_P108 "GSN wt Allele" @default.
- NCIT_C150252 NCIT_P208 "CL552044" @default.
- NCIT_C150252 NCIT_P321 "2934" @default.
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- NCIT_C150252 NCIT_R41 NCIT_C14250 @default.
- NCIT_C150252 NCIT_R41 NCIT_C14262 @default.
- NCIT_C150252 NCIT_R41 NCIT_C14282 @default.
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- NCIT_C150252 normalizedInformationContent "100" @default.
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- NCIT_C150252 hasExactSynonym "ADF" @default.
- NCIT_C150252 hasExactSynonym "AGEL" @default.
- NCIT_C150252 hasExactSynonym "Amyloidosis, Finnish Type Gene" @default.
- NCIT_C150252 hasExactSynonym "DKFZp313L0718" @default.
- NCIT_C150252 hasExactSynonym "GSN wt Allele" @default.
- NCIT_C150252 hasExactSynonym "Gelsolin (Amyloidosis, Finnish Type) Gene" @default.
- NCIT_C150252 hasExactSynonym "Gelsolin wt Allele" @default.
- NCIT_C150252 type Class @default.
- NCIT_C150252 isDefinedBy ncit.owl @default.
- NCIT_C150252 label "GSN wt Allele" @default.
- NCIT_C150252 subClassOf NCIT_C150249 @default.
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- NCIT_C150252 subClassOf NCIT_C16612 @default.
- NCIT_C150252 subClassOf NCIT_C20744 @default.
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