Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4127c5c3f2ea05b3d143eaf239b45d7f> ?p ?o ?g. }
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- B4127c5c3f2ea05b3d143eaf239b45d7f hasDbXref "Orphanet:2308" @default.
- B4127c5c3f2ea05b3d143eaf239b45d7f hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B4127c5c3f2ea05b3d143eaf239b45d7f type Axiom @default.
- B4127c5c3f2ea05b3d143eaf239b45d7f annotatedProperty IAO_0000115 @default.
- B4127c5c3f2ea05b3d143eaf239b45d7f annotatedSource MONDO_0007838 @default.
- B4127c5c3f2ea05b3d143eaf239b45d7f annotatedTarget "A multiple congenital anomaly/intellectual disability contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11." @default.