BRCA2 variants and cardiovascular disease in a multi-ethnic study. - Wikidata - awgldk - TriplyDB

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

http://www.wikidata.org/entity/Q34342912

about

rs15869 at miRNA binding site in BRCA2 is associated with breast cancer susceptibility.Ethnicity-Based Differences in the Association of LOXL1 Polymorphisms with Pseudoexfoliation/Pseudoexfoliative Glaucoma: A Meta-Analysis.

P2860

Q38733762-FCC24B13-33C6-404B-A135-C4DDB52D8EDC Q41319872-DC03908E-568B-48E5-8C2A-EAFCC5A4202F

P2860

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

http://www.wikidata.org/entity/Q34342912

description

2012 nî lūn-bûn

@nan

2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@ast

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@en

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@nl

type

label

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@ast

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@en

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@nl

prefLabel

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@ast

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@en

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@nl

P1433

Q34342912-225087C3-7ED3-41BB-8426-FDDB51FF151D

P1476

Q34342912-43938BF8-5507-4FD9-9392-E3D24F3194E6

P2093

Q34342912-111BD997-4A2A-4020-8BE1-8901B0005D9B

Q34342912-11A01352-C7C3-4ACC-B98F-C5A4844C6A78

Q34342912-2B87A6BE-B551-4B28-B670-42EA903E1D9A

Q34342912-2FC50FD9-8A1E-425E-BF60-E63B7622114F

Q34342912-4A90E702-AAE8-4A4F-A5D7-DC32679728ED

Q34342912-78544ED1-7DE4-4654-8AD7-A6EE23406F92

Q34342912-7F1902F0-AA39-4F11-B50E-168F34210EAC

Q34342912-8B2669B8-1357-4FF6-949A-86BD78C61261

Q34342912-A9356BA5-2C7D-4DD9-AEA3-25C8F7279F38

Q34342912-FAEA8AD5-A5C8-4817-AC3F-8895F1206B95

P2860

Q34342912-0CD89C61-78C7-4ABB-8DF2-DD1D3318CA73

Q34342912-13E0B3FD-C36E-4F36-976E-E8473C15595C

Q34342912-1F43A2AD-0DFB-465E-B8F0-1880534BBDBB

Q34342912-214F9C0A-8991-465E-BCC7-0F47ACA036C0

Q34342912-216C7D3D-A0C6-4127-A2B9-D65BE5BB1662

Q34342912-2D984B09-5171-4C75-8737-1916AE11048D

Q34342912-33958BAE-3E3A-46CC-8CD3-BF5031DE1989

Q34342912-47E20541-8718-46E6-B1E6-9EC99B59DF01

Q34342912-4D208706-F1EB-404D-8DE1-86C754148B32

Q34342912-5902BCB9-71A1-415E-9709-39CB66315908

P2888

Q34342912-03B203E0-FBFD-425D-BCDD-321B482C388E

P304

Q34342912-03262BF5-D55F-4415-A73F-1E966B1BDDD8

P31

Q34342912-15186f96-0ebc-4b17-9a38-603211ea2019

Q34342912-AD85191A-7C91-4781-BE2B-9AFD2D3B361B

P356

Q34342912-09D3C562-1AF4-4809-835C-01F23C8CCD69

P478

Q34342912-7CD854C0-75F9-44C0-AB48-4A11BEE453E8

P50

Q34342912-76469AC3-9CB7-4BC7-89CD-240F5E9D4FA8

Q34342912-9F925A41-1D93-4689-8375-78F31B949F9B

Q34342912-B97CAA50-FA64-4052-9108-12006F5733B0

P577

Q34342912-85B01A73-DAA2-4108-8F62-9DA3E8AF29CE

P5875

Q34342912-71356C69-FCF8-47A1-9F5D-AEB1243DC6F6

P6179

Q34342912-3283377A-BC98-4AD5-A632-FFB768497572

P698

Q34342912-4F8FC966-35B5-4536-9619-378C2BA2C0DD

P932

Q34342912-B35E3008-A1C2-46D8-B071-093BF38C7A25

P356

1471-2350-13-56

P1433

BMC Medical Genetics

P1476

BRCA2 variants and cardiovascular disease in a multi-ethnic study.

@en

P2093

A Darlene Davis

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

Changchun Xie

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

Guillaume Pare

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

James C Engert

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

John Danesh

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

Kevin Zbuk

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

Mahyar Heydarpour

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

Matthew B Lanktree

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

Robin Young

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

Ruby Miller

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

P2860

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies

BRCA1 is an essential regulator of heart function and survival following myocardial infarction

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

PLINK: a tool set for whole-genome association and population-based linkage analyses

Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS

Haploview: analysis and visualization of LD and haplotype maps

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study

A new multipoint method for genome-wide association studies by imputation of genotypes

P2888

1471-2350-13-56

P304

56

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

P31

scholarly article

P356

10.1186/1471-2350-13-56

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

P478

13

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

P50

Danish Saleheen

Robert A. Hegele

P577

2012-07-18T00:00:00Z

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

P5875

229324775

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

P6179

1025979655

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

P698

22809218

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

P932

3464815

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