Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B2156c4277f0a2a819426964d3833f25f> ?p ?o ?g. }
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- B2156c4277f0a2a819426964d3833f25f hasDbXref "https://clinicalgenome.org/affiliation/40006/" @default.
- B2156c4277f0a2a819426964d3833f25f type Axiom @default.
- B2156c4277f0a2a819426964d3833f25f annotatedProperty IAO_0000115 @default.
- B2156c4277f0a2a819426964d3833f25f annotatedSource MONDO_0100166 @default.
- B2156c4277f0a2a819426964d3833f25f annotatedTarget "Any intellectual disability in which the cause of the disease is a mutation in the PPP2R1A gene." @default.