Source:http://linkedlifedata.com/resource/pubmed/id/20738937
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
2010-8-26
|
pubmed:abstractText |
Coronary artery disease (CAD) has a substantial genetic component and, in recent years, a number of genetic variants associated with the disease have been identified. The objective of this study was to evaluate the magnitude of the association between a genetic risk score, which is based on the accumulated number of risk alleles in all genetic variants of interest, and the presence of CAD.
|
pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
1579-2242
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
63
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
925-33
|
pubmed:meshHeading | |
pubmed:year |
2010
|
pubmed:articleTitle |
Additive effect of multiple genetic variants on the risk of coronary artery disease.
|
pubmed:affiliation |
Grupo de Epidemiología y Genética Cardiovascular ULEC, Institut Municipal d'Investigació Mèdica, Hospital del Mar, Barcelona, España.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|