Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bcb75231067ce634a37d893032f7d1d60> ?p ?o ?g. }
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- Bcb75231067ce634a37d893032f7d1d60 hasDbXref "DOID:12583" @default.
- Bcb75231067ce634a37d893032f7d1d60 hasDbXref "PMID:PMID%3A+19243607" @default.
- Bcb75231067ce634a37d893032f7d1d60 type Axiom @default.
- Bcb75231067ce634a37d893032f7d1d60 annotatedProperty IAO_0000115 @default.
- Bcb75231067ce634a37d893032f7d1d60 annotatedSource MONDO_0008644 @default.
- Bcb75231067ce634a37d893032f7d1d60 annotatedTarget "A chromosomal disease that has material basis in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features." @default.