Rare variant of MAP2K7 is associated with increased risk of COPD in southern and eastern Chinese.

about

Rare variant of MAP2K7 is associated with increased risk of COPD in southern and eastern Chinese.

Item

http://www.wikidata.org/entity/Q39000705

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Rare variant of MAP2K7 is asso ...... southern and eastern Chinese.

@en

Rare variant of MAP2K7 is asso ...... southern and eastern Chinese.

@nl

type

Item

label

Rare variant of MAP2K7 is asso ...... southern and eastern Chinese.

@en

Rare variant of MAP2K7 is asso ...... southern and eastern Chinese.

@nl

prefLabel

Rare variant of MAP2K7 is asso ...... southern and eastern Chinese.

@en

Rare variant of MAP2K7 is asso ...... southern and eastern Chinese.

@nl

P1476

Rare variant of MAP2K7 is asso ...... southern and eastern Chinese.

@en

P2093

Chenli Xie

http://www.w3.org/2001/XMLSchema#string

Di Wu

http://www.w3.org/2001/XMLSchema#string

Fuman Qiu

http://www.w3.org/2001/XMLSchema#string

Jiachun Lu

http://www.w3.org/2001/XMLSchema#string

Jiansong Chen

http://www.w3.org/2001/XMLSchema#string

Lei Yang

http://www.w3.org/2001/XMLSchema#string

Qingqing Nong

http://www.w3.org/2001/XMLSchema#string

Xiaoxiao Lu

http://www.w3.org/2001/XMLSchema#string

Yifeng Zhou

http://www.w3.org/2001/XMLSchema#string

Yinyan Li

http://www.w3.org/2001/XMLSchema#string

P2860

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

The MKK7 p.Glu116Lys Rare Variant Serves as a Predictor for Lung Cancer Risk and Prognosis in Chinese.

Chronic obstructive pulmonary disease

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.

Differential expression of C-reactive protein and serum amyloid A in different cell types in the lung tissue of chronic obstructive pulmonary disease patients

Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits

Mechanistic links between COPD and lung cancer.

P304

691-698

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1111/RESP.12976

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-01-24T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28120412

http://www.w3.org/2001/XMLSchema#string

P921

chronic obstructive pulmonary disease