Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0ab99429edca50fd646b1f38c3f8e2f6> ?p ?o ?g. }
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- B0ab99429edca50fd646b1f38c3f8e2f6 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B0ab99429edca50fd646b1f38c3f8e2f6 type Axiom @default.
- B0ab99429edca50fd646b1f38c3f8e2f6 annotatedProperty IAO_0000115 @default.
- B0ab99429edca50fd646b1f38c3f8e2f6 annotatedSource MONDO_0014178 @default.
- B0ab99429edca50fd646b1f38c3f8e2f6 annotatedTarget "Any inclusion body myopathy with Paget disease of bone and frontotemporal dementia in which the cause of the disease is a mutation in the HNRNPA2B1 gene." @default.