Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3b78299bf0e7bd1992d289280d6b39a3> ?p ?o ?g. }
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- B3b78299bf0e7bd1992d289280d6b39a3 hasDbXref "SO:ke" @default.
- B3b78299bf0e7bd1992d289280d6b39a3 type Axiom @default.
- B3b78299bf0e7bd1992d289280d6b39a3 annotatedProperty IAO_0000115 @default.
- B3b78299bf0e7bd1992d289280d6b39a3 annotatedSource SO_0001880 @default.
- B3b78299bf0e7bd1992d289280d6b39a3 annotatedTarget "A sequence variant, caused by an alteration of the genomic sequence, where the structural change, an amplification of sequence, is greater than the extent of the underlying genomic features." @default.