Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B6ea05f42ab19b15d55ccc21d394161b3> ?p ?o ?g. }
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- B6ea05f42ab19b15d55ccc21d394161b3 hasDbXref "MONDO:design_pattern" @default.
- B6ea05f42ab19b15d55ccc21d394161b3 type Axiom @default.
- B6ea05f42ab19b15d55ccc21d394161b3 annotatedProperty hasExactSynonym @default.
- B6ea05f42ab19b15d55ccc21d394161b3 annotatedSource MONDO_0014178 @default.
- B6ea05f42ab19b15d55ccc21d394161b3 annotatedTarget "inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA2B1" @default.