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| pubmed-article:20698975 | lifeskim:mentions | umls-concept:C0702111 | lld:lifeskim |
| pubmed-article:20698975 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:20698975 | lifeskim:mentions | umls-concept:C0205396 | lld:lifeskim |
| pubmed-article:20698975 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:20698975 | pubmed:dateCreated | 2010-8-25 | lld:pubmed |
| pubmed-article:20698975 | pubmed:abstractText | Asthma is a chronic respiratory disease whose genetic basis has been explored for over two decades, most recently via genome-wide association studies. We sought to find asthma-susceptibility variants by using probands from a single population in both family-based and case-control association designs. | lld:pubmed |
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| pubmed-article:20698975 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:20698975 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20698975 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20698975 | pubmed:issn | 1471-2350 | lld:pubmed |
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| pubmed-article:20698975 | pubmed:author | pubmed-author:MurphyAmy JAJ | lld:pubmed |
| pubmed-article:20698975 | pubmed:author | pubmed-author:WuAnn CAC | lld:pubmed |
| pubmed-article:20698975 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20698975 | pubmed:volume | 11 | lld:pubmed |
| pubmed-article:20698975 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20698975 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20698975 | pubmed:pagination | 122 | lld:pubmed |
| pubmed-article:20698975 | pubmed:dateRevised | 2011-6-9 | lld:pubmed |
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| pubmed-article:20698975 | pubmed:year | 2010 | lld:pubmed |
