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| pubmed-article:19891555 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:19891555 | lifeskim:mentions | umls-concept:C0020538 | lld:lifeskim |
| pubmed-article:19891555 | lifeskim:mentions | umls-concept:C0018802 | lld:lifeskim |
| pubmed-article:19891555 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
| pubmed-article:19891555 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:19891555 | lifeskim:mentions | umls-concept:C1413865 | lld:lifeskim |
| pubmed-article:19891555 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:19891555 | pubmed:dateCreated | 2009-11-6 | lld:pubmed |
| pubmed-article:19891555 | pubmed:abstractText | We tested the hypothesis that genetic variation in vitamin D-dependent signaling is associated with congestive heart failure in human subjects with hypertension. | lld:pubmed |
| pubmed-article:19891555 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19891555 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19891555 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19891555 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19891555 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19891555 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:19891555 | pubmed:issn | 1744-8042 | lld:pubmed |
| pubmed-article:19891555 | pubmed:author | pubmed-author:McCartyCather... | lld:pubmed |
| pubmed-article:19891555 | pubmed:author | pubmed-author:MukeshBickol... | lld:pubmed |
| pubmed-article:19891555 | pubmed:author | pubmed-author:DartRichard... | lld:pubmed |
| pubmed-article:19891555 | pubmed:author | pubmed-author:WilkeRussell... | lld:pubmed |
| pubmed-article:19891555 | pubmed:author | pubmed-author:SimpsonRobert... | lld:pubmed |
| pubmed-article:19891555 | pubmed:author | pubmed-author:BhupathiSatya... | lld:pubmed |
| pubmed-article:19891555 | pubmed:author | pubmed-author:GhebraniousNa... | lld:pubmed |
| pubmed-article:19891555 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19891555 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:19891555 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19891555 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19891555 | pubmed:pagination | 1789-97 | lld:pubmed |
| pubmed-article:19891555 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
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| pubmed-article:19891555 | pubmed:meshHeading | pubmed-meshheading:19891555... | lld:pubmed |
| pubmed-article:19891555 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19891555 | pubmed:articleTitle | Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension. | lld:pubmed |
| pubmed-article:19891555 | pubmed:affiliation | Medical College of Wisconsin, WI, USA. | lld:pubmed |
| pubmed-article:19891555 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19891555 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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