Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B80cd1b21f11b5e3affe9ddc690d7abc9> ?p ?o ?g. }
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- B80cd1b21f11b5e3affe9ddc690d7abc9 hasDbXref "MONDO:design_pattern" @default.
- B80cd1b21f11b5e3affe9ddc690d7abc9 type Axiom @default.
- B80cd1b21f11b5e3affe9ddc690d7abc9 annotatedProperty hasExactSynonym @default.
- B80cd1b21f11b5e3affe9ddc690d7abc9 annotatedSource MONDO_0014178 @default.
- B80cd1b21f11b5e3affe9ddc690d7abc9 annotatedTarget "inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA2B1" @default.