Source:http://linkedlifedata.com/resource/pubmed/id/15571588
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
12
|
| pubmed:dateCreated |
2004-12-1
|
| pubmed:abstractText |
Three variants of the CARD15/NOD2 gene (SNP8, SNP12, and SNP13) have been associated with Crohn's disease (CD). We assessed the impact of NOD2 variants on the CD risk across diverse populations and examined possible associations with disease phenotype.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Dec
|
| pubmed:issn |
0002-9270
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
99
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
2393-404
|
| pubmed:dateRevised |
2008-5-13
|
| pubmed:meshHeading |
pubmed-meshheading:15571588-Chi-Square Distribution,
pubmed-meshheading:15571588-Crohn Disease,
pubmed-meshheading:15571588-Genetic Predisposition to Disease,
pubmed-meshheading:15571588-Humans,
pubmed-meshheading:15571588-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:15571588-Nod2 Signaling Adaptor Protein,
pubmed-meshheading:15571588-Phenotype,
pubmed-meshheading:15571588-Risk Assessment
|
| pubmed:year |
2004
|
| pubmed:articleTitle |
Differential effects of NOD2 variants on Crohn's disease risk and phenotype in diverse populations: a metaanalysis.
|
| pubmed:affiliation |
Department of Medicine, 1st Division of Internal Medicine and Hepato-Gastroenterology Unit, University Hospital, University of Ioannina School of Medicine, Ioannina 45110, Greece.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Meta-Analysis
|