uracil-N-glycosylase drug
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| uracil-N-glycosylase | associated_with | SLC1A1 | — | 1 |
Mentioned in (2)
Papers in which this entity is mentioned.
- Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. (2013)
- A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder. (2009)
Merged raw entities (1)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| uracil-n-glycosylase | drug | 2 | 3 |