Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B958effdda918a7cf8968139b4542e67f> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B958effdda918a7cf8968139b4542e67f hasDbXref "NCIT:C128806" @default.
- B958effdda918a7cf8968139b4542e67f type Axiom @default.
- B958effdda918a7cf8968139b4542e67f annotatedProperty IAO_0000115 @default.
- B958effdda918a7cf8968139b4542e67f annotatedSource MONDO_0015903 @default.
- B958effdda918a7cf8968139b4542e67f annotatedTarget "An autosomal dominant genetic condition caused by mutation(s) in the CETP gene, encoding cholesteryl ester transfer protein. Affected individuals may have increased longevity due to decreased risk of coronary heart disease." @default.