pubmed-article:19141580 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19141580 | lifeskim:mentions | umls-concept:C0011860 | lld:lifeskim |
pubmed-article:19141580 | lifeskim:mentions | umls-concept:C1333572 | lld:lifeskim |
pubmed-article:19141580 | lifeskim:mentions | umls-concept:C1969875 | lld:lifeskim |
pubmed-article:19141580 | lifeskim:mentions | umls-concept:C0271650 | lld:lifeskim |
pubmed-article:19141580 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
pubmed-article:19141580 | lifeskim:mentions | umls-concept:C0004083 | lld:lifeskim |
pubmed-article:19141580 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
pubmed-article:19141580 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:19141580 | pubmed:dateCreated | 2009-4-7 | lld:pubmed |
pubmed-article:19141580 | pubmed:abstractText | The transcription factor forkhead box protein (FOX) O1A plays a crucial role in regulation of beta-cell function and metabolic effects of insulin in the liver. | lld:pubmed |
pubmed-article:19141580 | pubmed:language | eng | lld:pubmed |
pubmed-article:19141580 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19141580 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:19141580 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19141580 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19141580 | pubmed:month | Apr | lld:pubmed |
pubmed-article:19141580 | pubmed:issn | 1945-7197 | lld:pubmed |
pubmed-article:19141580 | pubmed:author | pubmed-author:ThamerClausC | lld:pubmed |
pubmed-article:19141580 | pubmed:author | pubmed-author:MachicaoFaust... | lld:pubmed |
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pubmed-article:19141580 | pubmed:author | pubmed-author:SchickFritzF | lld:pubmed |
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pubmed-article:19141580 | pubmed:author | pubmed-author:MüssigKarsten... | lld:pubmed |
pubmed-article:19141580 | pubmed:author | pubmed-author:StancákováAle... | lld:pubmed |
pubmed-article:19141580 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19141580 | pubmed:volume | 94 | lld:pubmed |
pubmed-article:19141580 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19141580 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19141580 | pubmed:pagination | 1353-60 | lld:pubmed |
pubmed-article:19141580 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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pubmed-article:19141580 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19141580 | pubmed:articleTitle | Association of common genetic variation in the FOXO1 gene with beta-cell dysfunction, impaired glucose tolerance, and type 2 diabetes. | lld:pubmed |
pubmed-article:19141580 | pubmed:affiliation | Department of Diagnostic Radiology, Division of Endocrinology, University Hospital of Tü bingen, Tübingen, Germany. | lld:pubmed |
pubmed-article:19141580 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19141580 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:19141580 | pubmed:publicationType | Multicenter Study | lld:pubmed |
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