Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B769288ba174def0d5bcc9247d873e017> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B769288ba174def0d5bcc9247d873e017 hasDbXref "MONDO:patterns/hereditary" @default.
- B769288ba174def0d5bcc9247d873e017 type Axiom @default.
- B769288ba174def0d5bcc9247d873e017 annotatedProperty IAO_0000115 @default.
- B769288ba174def0d5bcc9247d873e017 annotatedSource MONDO_0019118 @default.
- B769288ba174def0d5bcc9247d873e017 annotatedTarget "An instance of retinal degeneration that is caused by an inherited modification of the individual's genome." @default.