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- Bfad19fe255b6e34f6b2d008a40429186 NCIT_P378 "NCI" @default.
- Bfad19fe255b6e34f6b2d008a40429186 type Axiom @default.
- Bfad19fe255b6e34f6b2d008a40429186 annotatedProperty IAO_0000115 @default.
- Bfad19fe255b6e34f6b2d008a40429186 annotatedSource NCIT_C49357 @default.
- Bfad19fe255b6e34f6b2d008a40429186 annotatedTarget "Human EPHX1 wild-type allele is located in the vicinity of 1q42.1 and is approximately 35 kb in length. This allele, which encodes epoxide hydrolase 1 protein, is involved in the metabolism of both arene and aliphatic epoxides. Certain allelic variants of the EPHX1 gene confer susceptibility to lymphoproliferative disorders. Specific inherited defects in this gene also cause familial hypercholanemia. An EPHX1 low-activity genotype is associated with decreased risk of lung cancer." @default.