Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf1a793561e9d3228a3e1e67a27f5cdc7> ?p ?o ?g. }
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- Bf1a793561e9d3228a3e1e67a27f5cdc7 hasDbXref "NCBI:th" @default.
- Bf1a793561e9d3228a3e1e67a27f5cdc7 type Axiom @default.
- Bf1a793561e9d3228a3e1e67a27f5cdc7 annotatedProperty IAO_0000115 @default.
- Bf1a793561e9d3228a3e1e67a27f5cdc7 annotatedSource SO_0002007 @default.
- Bf1a793561e9d3228a3e1e67a27f5cdc7 annotatedTarget "An MNV is a multiple nucleotide variant (substitution) in which the inserted sequence is the same length as the replaced sequence." @default.