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| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C0006142 | lld:lifeskim |
| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C0596244 | lld:lifeskim |
| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C0004083 | lld:lifeskim |
| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C1285573 | lld:lifeskim |
| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:17598925 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
| pubmed-article:17598925 | pubmed:dateCreated | 2007-7-20 | lld:pubmed |
| pubmed-article:17598925 | pubmed:abstractText | Copy number polymorphisms caused by genomic rearrangements like deletions, make a significant contribution to the genomic differences between two individuals and may add to disease predisposition. Therefore, genotyping of such deletion polymorphisms in case-control studies could give important insights into risk associations. | lld:pubmed |
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| pubmed-article:17598925 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:17598925 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:17598925 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17598925 | pubmed:issn | 1471-2156 | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:HemminkiKariK | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:GrzybowskaEwa... | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:FörstiAstaA | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:ButkiewiczDor... | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:WagnerKerstin... | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:PekalaWiolett... | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:Pamula-PilatJ... | lld:pubmed |
| pubmed-article:17598925 | pubmed:author | pubmed-author:TeczaKarolina... | lld:pubmed |
| pubmed-article:17598925 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:17598925 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:17598925 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17598925 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17598925 | pubmed:pagination | 41 | lld:pubmed |
| pubmed-article:17598925 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:17598925 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17598925 | pubmed:articleTitle | High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk. | lld:pubmed |
| pubmed-article:17598925 | pubmed:affiliation | Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, Heidelberg, Germany. wagner_ke@yahoo.de <wagner_ke@yahoo.de> | lld:pubmed |
| pubmed-article:17598925 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17598925 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:154754 | entrezgene:pubmed | pubmed-article:17598925 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:17598925 | lld:entrezgene |
| lhgdn:association:4043 | lhgdn:found_in | pubmed-article:17598925 | lld:lhgdn |
