| pubmed-article:20638926 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20638926 | lifeskim:mentions | umls-concept:C0006142 | lld:lifeskim |
| pubmed-article:20638926 | lifeskim:mentions | umls-concept:C0035648 | lld:lifeskim |
| pubmed-article:20638926 | lifeskim:mentions | umls-concept:C1417387 | lld:lifeskim |
| pubmed-article:20638926 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:20638926 | lifeskim:mentions | umls-concept:C0242303 | lld:lifeskim |
| pubmed-article:20638926 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:20638926 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:20638926 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:20638926 | pubmed:dateCreated | 2010-10-4 | lld:pubmed |
| pubmed-article:20638926 | pubmed:abstractText | The aim of this study was to investigate the association of a 11 nucleotide deletion, the c.469+46_56del mutation, in the intron of the homeobox MSX1 gene and breast cancer occurrence and characteristics. | lld:pubmed |
| pubmed-article:20638926 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20638926 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20638926 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:20638926 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20638926 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20638926 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20638926 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:20638926 | pubmed:issn | 1877-783X | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:BlasiakJanusz... | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:MorawiecZbign... | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:SliwinskiToma... | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:SynowiecEweli... | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:FormaEwaE | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:DzikiLukaszL | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:CzarnyPiotrP | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:GomulakPaulin... | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:MorawiecJanJ | lld:pubmed |
| pubmed-article:20638926 | pubmed:author | pubmed-author:WasyleckaMaja... | lld:pubmed |
| pubmed-article:20638926 | pubmed:copyrightInfo | Copyright © 2010 Elsevier Ltd. All rights reserved. | lld:pubmed |
| pubmed-article:20638926 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20638926 | pubmed:volume | 34 | lld:pubmed |
| pubmed-article:20638926 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20638926 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20638926 | pubmed:pagination | 652-5 | lld:pubmed |
| pubmed-article:20638926 | pubmed:dateRevised | 2011-6-17 | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
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| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
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| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:meshHeading | pubmed-meshheading:20638926... | lld:pubmed |
| pubmed-article:20638926 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20638926 | pubmed:articleTitle | The c.469+46_56del mutation in the homeobox MSX1 gene--a novel risk factor in breast cancer? | lld:pubmed |
| pubmed-article:20638926 | pubmed:affiliation | Department of Molecular Genetics, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland. | lld:pubmed |
| pubmed-article:20638926 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20638926 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:4487 | entrezgene:pubmed | pubmed-article:20638926 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20638926 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20638926 | lld:entrezgene |
