pubmed-article:17101573 | rdf:type | pubmed:Citation | lld:pubmed |
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pubmed-article:17101573 | lifeskim:mentions | umls-concept:C0681890 | lld:lifeskim |
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pubmed-article:17101573 | lifeskim:mentions | umls-concept:C0332183 | lld:lifeskim |
pubmed-article:17101573 | lifeskim:mentions | umls-concept:C0332167 | lld:lifeskim |
pubmed-article:17101573 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:17101573 | pubmed:dateCreated | 2006-11-14 | lld:pubmed |
pubmed-article:17101573 | pubmed:abstractText | The identification of CARD15 as a susceptibility gene for Crohn's disease (CD) offers new possibilities for patient classification and risk assessment. The purpose of this study was to carry out a CARD15 sequence analysis in a large single-center IBD cohort and to investigate the impact of different genotypes on disease phenotypes. | lld:pubmed |
pubmed-article:17101573 | pubmed:language | eng | lld:pubmed |
pubmed-article:17101573 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17101573 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17101573 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17101573 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17101573 | pubmed:month | Dec | lld:pubmed |
pubmed-article:17101573 | pubmed:issn | 0036-5521 | lld:pubmed |
pubmed-article:17101573 | pubmed:author | pubmed-author:BrandStephanS | lld:pubmed |
pubmed-article:17101573 | pubmed:author | pubmed-author:LohsePeterP | lld:pubmed |
pubmed-article:17101573 | pubmed:author | pubmed-author:GökeBurkhardB | lld:pubmed |
pubmed-article:17101573 | pubmed:author | pubmed-author:SackmannMicha... | lld:pubmed |
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pubmed-article:17101573 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17101573 | pubmed:volume | 41 | lld:pubmed |
pubmed-article:17101573 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17101573 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17101573 | pubmed:pagination | 1421-32 | lld:pubmed |
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pubmed-article:17101573 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:17101573 | pubmed:articleTitle | Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis. | lld:pubmed |
pubmed-article:17101573 | pubmed:affiliation | Department of Internal Medicine II, University of Munich, Germany. | lld:pubmed |
pubmed-article:17101573 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17101573 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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