Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bfdec0adac460f14116d9acd6703fc737> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bfdec0adac460f14116d9acd6703fc737 NCIT_P378 "NCI" @default.
- Bfdec0adac460f14116d9acd6703fc737 type Axiom @default.
- Bfdec0adac460f14116d9acd6703fc737 annotatedProperty IAO_0000115 @default.
- Bfdec0adac460f14116d9acd6703fc737 annotatedSource NCIT_C105077 @default.
- Bfdec0adac460f14116d9acd6703fc737 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.