CHB+JPT drug
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| HapMap | associated_with | CHB+JPT | — | 1 |
Mentioned in (5)
Papers in which this entity is mentioned.
- Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
- Identification of CHRNA5 rare variants in African-American heavy smokers. (2014)
- Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. (2013)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
- A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. (2006)
Merged raw entities (5)
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 |
|---|---|---|---|
| chb+jpt | cohort | 5 | 13 |
| chb | drug | — | — |
| chb+jpt | drug | — | — |
| east asian (chb+jpt) | drug | — | — |
| jpt | drug | — | — |