Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B23f85a06b1c81e9709f3afd5a45704cc> ?p ?o ?g. }
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- B23f85a06b1c81e9709f3afd5a45704cc hasDbXref "NCIT:P378" @default.
- B23f85a06b1c81e9709f3afd5a45704cc type Axiom @default.
- B23f85a06b1c81e9709f3afd5a45704cc annotatedProperty IAO_0000115 @default.
- B23f85a06b1c81e9709f3afd5a45704cc annotatedSource MONDO_0010383 @default.
- B23f85a06b1c81e9709f3afd5a45704cc annotatedTarget "A genetic syndrome caused by mutations in the FMR1 gene which is responsible for the expression of the fragile X mental retardation 1 protein. This protein participates in neural development. This syndrome is manifested with mental, emotional, behavioral, physical, and learning disabilities." @default.