Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bbf36ea32731b1802ffc578e8b45fede1> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bbf36ea32731b1802ffc578e8b45fede1 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- Bbf36ea32731b1802ffc578e8b45fede1 type Axiom @default.
- Bbf36ea32731b1802ffc578e8b45fede1 annotatedProperty IAO_0000115 @default.
- Bbf36ea32731b1802ffc578e8b45fede1 annotatedSource MONDO_0013482 @default.
- Bbf36ea32731b1802ffc578e8b45fede1 annotatedTarget "Any Meckel syndrome in which the cause of the disease is a mutation in the TCTN2 gene." @default.