| pubmed-article:17562002 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17562002 | lifeskim:mentions | umls-concept:C0005516 | lld:lifeskim |
| pubmed-article:17562002 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
| pubmed-article:17562002 | lifeskim:mentions | umls-concept:C0597198 | lld:lifeskim |
| pubmed-article:17562002 | lifeskim:mentions | umls-concept:C0036849 | lld:lifeskim |
| pubmed-article:17562002 | lifeskim:mentions | umls-concept:C0680536 | lld:lifeskim |
| pubmed-article:17562002 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
| pubmed-article:17562002 | pubmed:dateCreated | 2007-7-13 | lld:pubmed |
| pubmed-article:17562002 | pubmed:abstractText | New technologies have enabled genome-wide association studies to be conducted with hundreds of thousands of genotyped SNPs. Several different first-generation genome-wide panels of SNPs have been commercialized. The total amount of common genetic variation is still unknown; however, the coverage of commercial panels can be evaluated against reference population samples genotyped by the International HapMap project. Less information is available about coverage in samples from other populations. | lld:pubmed |
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| pubmed-article:17562002 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17562002 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17562002 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:17562002 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17562002 | pubmed:issn | 1471-2164 | lld:pubmed |
| pubmed-article:17562002 | pubmed:author | pubmed-author:MetspaluAndre... | lld:pubmed |
| pubmed-article:17562002 | pubmed:author | pubmed-author:RemmMaidoM | lld:pubmed |
| pubmed-article:17562002 | pubmed:author | pubmed-author:MontpetitAlex... | lld:pubmed |
| pubmed-article:17562002 | pubmed:author | pubmed-author:MägiReedikR | lld:pubmed |
| pubmed-article:17562002 | pubmed:author | pubmed-author:PfeuferArneA | lld:pubmed |
| pubmed-article:17562002 | pubmed:author | pubmed-author:NelisMariM | lld:pubmed |
| pubmed-article:17562002 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:17562002 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:17562002 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17562002 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17562002 | pubmed:pagination | 159 | lld:pubmed |
| pubmed-article:17562002 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:17562002 | pubmed:meshHeading | pubmed-meshheading:17562002... | lld:pubmed |
| pubmed-article:17562002 | pubmed:meshHeading | pubmed-meshheading:17562002... | lld:pubmed |
| pubmed-article:17562002 | pubmed:meshHeading | pubmed-meshheading:17562002... | lld:pubmed |
| pubmed-article:17562002 | pubmed:meshHeading | pubmed-meshheading:17562002... | lld:pubmed |
| pubmed-article:17562002 | pubmed:meshHeading | pubmed-meshheading:17562002... | lld:pubmed |
| pubmed-article:17562002 | pubmed:meshHeading | pubmed-meshheading:17562002... | lld:pubmed |
| pubmed-article:17562002 | pubmed:meshHeading | pubmed-meshheading:17562002... | lld:pubmed |
| pubmed-article:17562002 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17562002 | pubmed:articleTitle | Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation. | lld:pubmed |
| pubmed-article:17562002 | pubmed:affiliation | Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia. reedik.magi@ut.ee <reedik.magi@ut.ee> | lld:pubmed |
| pubmed-article:17562002 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17562002 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:17562002 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
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