pubmed-article:19329499 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19329499 | lifeskim:mentions | umls-concept:C0018801 | lld:lifeskim |
pubmed-article:19329499 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
pubmed-article:19329499 | lifeskim:mentions | umls-concept:C1515498 | lld:lifeskim |
pubmed-article:19329499 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
pubmed-article:19329499 | lifeskim:mentions | umls-concept:C0314603 | lld:lifeskim |
pubmed-article:19329499 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:19329499 | lifeskim:mentions | umls-concept:C1551358 | lld:lifeskim |
pubmed-article:19329499 | pubmed:issue | 10 | lld:pubmed |
pubmed-article:19329499 | pubmed:dateCreated | 2009-5-15 | lld:pubmed |
pubmed-article:19329499 | pubmed:abstractText | Recent studies showed that polymorphisms on chromosome 9p21 are associated with coronary heart disease (CHD), but few studies examined the association with heart failure (HF), stroke, or other subclinical atherosclerotic diseases. We tested the association of chromosome 9p21 polymorphisms with non-coronary atherosclerotic diseases. | lld:pubmed |
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pubmed-article:19329499 | pubmed:language | eng | lld:pubmed |
pubmed-article:19329499 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19329499 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19329499 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19329499 | pubmed:month | May | lld:pubmed |
pubmed-article:19329499 | pubmed:issn | 1522-9645 | lld:pubmed |
pubmed-article:19329499 | pubmed:author | pubmed-author:RosamondWayne... | lld:pubmed |
pubmed-article:19329499 | pubmed:author | pubmed-author:BoerwinkleEri... | lld:pubmed |
pubmed-article:19329499 | pubmed:author | pubmed-author:FolsomAaron... | lld:pubmed |
pubmed-article:19329499 | pubmed:author | pubmed-author:ARIC... | lld:pubmed |
pubmed-article:19329499 | pubmed:author | pubmed-author:YamagishiKazu... | lld:pubmed |
pubmed-article:19329499 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19329499 | pubmed:volume | 30 | lld:pubmed |
pubmed-article:19329499 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19329499 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19329499 | pubmed:pagination | 1222-8 | lld:pubmed |
pubmed-article:19329499 | pubmed:dateRevised | 2010-9-23 | lld:pubmed |
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pubmed-article:19329499 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19329499 | pubmed:articleTitle | A genetic variant on chromosome 9p21 and incident heart failure in the ARIC study. | lld:pubmed |
pubmed-article:19329499 | pubmed:affiliation | Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, 1300 S Second Street, Suite 300, Minneapolis, MN 55454-1015, USA. | lld:pubmed |
pubmed-article:19329499 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19329499 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:19329499 | pubmed:publicationType | Multicenter Study | lld:pubmed |
pubmed-article:19329499 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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