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| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0683983 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0035647 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0009462 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C1335837 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C1705603 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0004153 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0001925 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0017725 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C0007328 | lld:lifeskim |
| pubmed-article:21247498 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:21247498 | pubmed:dateCreated | 2011-2-8 | lld:pubmed |
| pubmed-article:21247498 | pubmed:abstractText | Evidence suggests glucose transporter-1 (GLUT1) genetic variation affects diabetic nephropathy and albuminuria. Our aim was to evaluate associations with albuminuria of six GLUT1 single nucleotide polymorphisms(SNPs), particularly XbaI and the previously associated Enhancer-2 (Enh2) SNP. | lld:pubmed |
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| pubmed-article:21247498 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21247498 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21247498 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:21247498 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21247498 | pubmed:issn | 1471-2350 | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:CoreshJosefJ | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:ShuldinerAlan... | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:SteffesMichae... | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:BrancatiFrede... | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:HeiligCharles... | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:HsuCharles... | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:BoerwinkleEri... | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:KaoWenhong... | lld:pubmed |
| pubmed-article:21247498 | pubmed:author | pubmed-author:GambirTejalT | lld:pubmed |
| pubmed-article:21247498 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21247498 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:21247498 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21247498 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21247498 | pubmed:pagination | 16 | lld:pubmed |
| pubmed-article:21247498 | pubmed:dateRevised | 2011-7-25 | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
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| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:meshHeading | pubmed-meshheading:21247498... | lld:pubmed |
| pubmed-article:21247498 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21247498 | pubmed:articleTitle | Genetic variation of glucose transporter-1 (GLUT1) and albuminuria in 10,278 European Americans and African Americans: a case-control study in the Atherosclerosis Risk in Communities (ARIC) study. | lld:pubmed |
| pubmed-article:21247498 | pubmed:affiliation | Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA. | lld:pubmed |
| pubmed-article:21247498 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21247498 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:21247498 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| entrez-gene:10755 | entrezgene:pubmed | pubmed-article:21247498 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21247498 | lld:entrezgene |
