Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B37c4e3bf238b6e73cd7f9754a689dd6a> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B37c4e3bf238b6e73cd7f9754a689dd6a hasDbXref "MONDO:patterns/hereditary" @default.
- B37c4e3bf238b6e73cd7f9754a689dd6a type Axiom @default.
- B37c4e3bf238b6e73cd7f9754a689dd6a annotatedProperty IAO_0000115 @default.
- B37c4e3bf238b6e73cd7f9754a689dd6a annotatedSource MONDO_0043007 @default.
- B37c4e3bf238b6e73cd7f9754a689dd6a annotatedTarget "OBSOLETE. An instance of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome that is caused by an inherited modification of the individual's genome." @default.