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- Bcd26f9f130d72f69bf38fb35a2c15935 NCIT_P378 "NCI" @default.
- Bcd26f9f130d72f69bf38fb35a2c15935 type Axiom @default.
- Bcd26f9f130d72f69bf38fb35a2c15935 annotatedProperty IAO_0000115 @default.
- Bcd26f9f130d72f69bf38fb35a2c15935 annotatedSource NCIT_C49413 @default.
- Bcd26f9f130d72f69bf38fb35a2c15935 annotatedTarget "Human WRN wild-type allele is located within 8p12-p11.2 and is approximately 140 kb in length. This allele, which encodes Werner syndrome ATP-dependent helicase protein, is involved in the both the formation of DNA replication focal centers and the unwinding of single- and double-stranded DNA in a 3'-5' direction. Certain allelic variants of this gene cause Werner syndrome." @default.