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- NCIT_C177196 IAO_0000115 "Human FAH wild-type allele is located in the vicinity of 15q25.1 and is approximately 34 kb in length. This allele, which encodes fumarylacetoacetase protein, plays a role in tyrosine degradation. Mutation of the gene is associated with tyrosinemia type 1." @default.
- NCIT_C177196 NCIT_NHC0 "C177196" @default.
- NCIT_C177196 NCIT_P100 "613871" @default.
- NCIT_C177196 NCIT_P102 "M55150" @default.
- NCIT_C177196 NCIT_P106 "Gene or Genome" @default.
- NCIT_C177196 NCIT_P108 "FAH wt Allele" @default.
- NCIT_C177196 NCIT_P208 "CL1643032" @default.
- NCIT_C177196 NCIT_P321 "2184" @default.
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- NCIT_C177196 normalizedInformationContent "100" @default.
- NCIT_C177196 referenceCount "1" @default.
- NCIT_C177196 hasExactSynonym "FAH wt Allele" @default.
- NCIT_C177196 hasExactSynonym "Fumarylacetoacetate Hydrolase (Fumarylacetoacetase) Gene" @default.
- NCIT_C177196 hasExactSynonym "Fumarylacetoacetate Hydrolase wt Allele" @default.
- NCIT_C177196 type Class @default.
- NCIT_C177196 isDefinedBy ncit.owl @default.
- NCIT_C177196 label "FAH wt Allele" @default.
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- NCIT_C177196 subClassOf NCIT_C21281 @default.
- NCIT_C177196 subClassOf NCIT_C25804 @default.