disease risk phenotype
Evidence from:
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No related entities found.
Mentioned in (6)
Papers in which this entity is mentioned.
- The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Enter the Matrix: Factorization Uncovers Knowledge from Omics. (2018)
- Annotation-free quantification of RNA splicing using LeafCutter. (2018)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
Merged raw entities (2)
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 |
|---|---|---|---|
| disease risk | phenotype | 27 | 31 |
| disease risks | phenotype | 1 | 1 |