Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bbe108e51a10ef30710388880dbe0abe1> ?p ?o ?g. }
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- Bbe108e51a10ef30710388880dbe0abe1 hasDbXref "Orphanet:2308" @default.
- Bbe108e51a10ef30710388880dbe0abe1 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- Bbe108e51a10ef30710388880dbe0abe1 type Axiom @default.
- Bbe108e51a10ef30710388880dbe0abe1 annotatedProperty IAO_0000115 @default.
- Bbe108e51a10ef30710388880dbe0abe1 annotatedSource MONDO_0007838 @default.
- Bbe108e51a10ef30710388880dbe0abe1 annotatedTarget "A multiple congenital anomaly/intellectual disability contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11." @default.