Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B6cca42ee9cceff42a7d56a3dc6be6607> ?p ?o ?g. }
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- B6cca42ee9cceff42a7d56a3dc6be6607 hasDbXref "SO:ke" @default.
- B6cca42ee9cceff42a7d56a3dc6be6607 type Axiom @default.
- B6cca42ee9cceff42a7d56a3dc6be6607 annotatedProperty IAO_0000115 @default.
- B6cca42ee9cceff42a7d56a3dc6be6607 annotatedSource SO_0001882 @default.
- B6cca42ee9cceff42a7d56a3dc6be6607 annotatedTarget "A sequence variant, caused by an alteration of the genomic sequence, where a deletion fuses genomic features." @default.