Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4c697372ff8ece6ef1b2f1199fea5ce3> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B4c697372ff8ece6ef1b2f1199fea5ce3 hasDbXref "MONDO:design_pattern" @default.
- B4c697372ff8ece6ef1b2f1199fea5ce3 type Axiom @default.
- B4c697372ff8ece6ef1b2f1199fea5ce3 annotatedProperty hasExactSynonym @default.
- B4c697372ff8ece6ef1b2f1199fea5ce3 annotatedSource MONDO_0013657 @default.
- B4c697372ff8ece6ef1b2f1199fea5ce3 annotatedTarget "autosomal dominant non-syndromic intellectual disability caused by mutation in CACNG2" @default.