disease genes gene
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| disease genes | associated_with | disease | — | 1 |
| families | associated_with | disease genes | — | 1 |
Mentioned in (11)
Papers in which this entity is mentioned.
- High-Parameter Spatial Multi-Omics through Histology-Anchored Integration (2025)
- Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
- Genetic effects on gene expression across human tissues. (2017)
- Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines. (2017)
- Guidelines for investigating causality of sequence variants in human disease. (2014)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Network of Cancer Genes: a web resource to analyze duplicability, orthology and network properties of cancer genes. (2010)
- ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. (2009)
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. (2009)
- ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. (2009)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
Merged raw entities (3)
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 genes | gene | 5 | 5 |
| disease-related genes | gene | 4 | 4 |
| disease genes | cohort | 2 | 2 |