narrow-sense heritability phenotype
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| families | associated_with | narrow-sense heritability | — | 1 |
| narrow-sense heritability | biomarker_for | transcript | — | 1 |
| non-additive genetic effects | risk_factor_for | narrow-sense heritability | — | 1 |
Mentioned in (5)
Papers in which this entity is mentioned.
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
- A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. (2013)
- Finding the missing heritability of complex diseases. (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 |
|---|---|---|---|
| narrow-sense heritability | phenotype | 5 | 5 |