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- Bf79f427e68a7acc5a6fe90382cd9d5ca NCIT_P378 "NCI" @default.
- Bf79f427e68a7acc5a6fe90382cd9d5ca type Axiom @default.
- Bf79f427e68a7acc5a6fe90382cd9d5ca annotatedProperty IAO_0000115 @default.
- Bf79f427e68a7acc5a6fe90382cd9d5ca annotatedSource NCIT_C105077 @default.
- Bf79f427e68a7acc5a6fe90382cd9d5ca annotatedTarget "Human SOST wild-type allele is located in the vicinity of 17q11.2 and is approximately 5 kb in length. This allele, which encodes sclerostin protein, is involved in the negative regulation of ossification. Mutation of the gene is associated with bone dysplasias including sclerosteosis type 1, van Buchem disease and craniodiaphyseal dysplasia autosomal dominant." @default.