Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B7689979021d26b33a5dbfc97ca943f04> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B7689979021d26b33a5dbfc97ca943f04 NCIT_P378 "NCI" @default.
- B7689979021d26b33a5dbfc97ca943f04 type Axiom @default.
- B7689979021d26b33a5dbfc97ca943f04 annotatedProperty IAO_0000115 @default.
- B7689979021d26b33a5dbfc97ca943f04 annotatedSource NCIT_C3447 @default.
- B7689979021d26b33a5dbfc97ca943f04 annotatedTarget "A rare, autosomal recessive syndrome caused by mutations in the WRN gene. It is characterized by the appearance of accelerated aging following puberty. It is associated with the development of diabetes mellitus, atherosclerosis, cataracts, and cancer." @default.