| pubmed-article:18647954 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18647954 | lifeskim:mentions | umls-concept:C1551488 | lld:lifeskim |
| pubmed-article:18647954 | lifeskim:mentions | umls-concept:C0011860 | lld:lifeskim |
| pubmed-article:18647954 | lifeskim:mentions | umls-concept:C0021655 | lld:lifeskim |
| pubmed-article:18647954 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:18647954 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:18647954 | lifeskim:mentions | umls-concept:C1833334 | lld:lifeskim |
| pubmed-article:18647954 | lifeskim:mentions | umls-concept:C1421976 | lld:lifeskim |
| pubmed-article:18647954 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:18647954 | pubmed:dateCreated | 2008-10-30 | lld:pubmed |
| pubmed-article:18647954 | pubmed:abstractText | A prior genome-wide association (GWA) study in Pima Indians identified variants within PCLO that were associated with early-onset type 2 diabetes. PCLO encodes a presynaptic cytomatrix protein that functions as a Ca(2+) sensor that may be involved in insulin secretion and/or insulin action. Therefore, PCLO was analyzed as a candidate gene for type 2 diabetes. | lld:pubmed |
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| pubmed-article:18647954 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18647954 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18647954 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:18647954 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18647954 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:18647954 | pubmed:issn | 1939-327X | lld:pubmed |
| pubmed-article:18647954 | pubmed:author | pubmed-author:RaoD CDC | lld:pubmed |
| pubmed-article:18647954 | pubmed:author | pubmed-author:LillyNN | lld:pubmed |
| pubmed-article:18647954 | pubmed:author | pubmed-author:BogardusClift... | lld:pubmed |
| pubmed-article:18647954 | pubmed:author | pubmed-author:HansonRobert... | lld:pubmed |
| pubmed-article:18647954 | pubmed:author | pubmed-author:BaierLeslie... | lld:pubmed |
| pubmed-article:18647954 | pubmed:author | pubmed-author:KobesSayukoS | lld:pubmed |
| pubmed-article:18647954 | pubmed:author | pubmed-author:QueLorem NLN | lld:pubmed |
| pubmed-article:18647954 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18647954 | pubmed:volume | 57 | lld:pubmed |
| pubmed-article:18647954 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18647954 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18647954 | pubmed:pagination | 3156-60 | lld:pubmed |
| pubmed-article:18647954 | pubmed:dateRevised | 2010-9-21 | lld:pubmed |
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| pubmed-article:18647954 | pubmed:meshHeading | pubmed-meshheading:18647954... | lld:pubmed |
| pubmed-article:18647954 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18647954 | pubmed:articleTitle | PCLO variants are nominally associated with early-onset type 2 diabetes and insulin resistance in Pima Indians. | lld:pubmed |
| pubmed-article:18647954 | pubmed:affiliation | Department of Health and HumanServices, Diabetes Molecular Genetics Section, Phoenix Epidemiology and Clinical Research Branch, National Institute of Diabetes and Digestive and KidneyDiseases, National Institutes of Health, Phoenix, Arizona, USA. | lld:pubmed |
| pubmed-article:18647954 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18647954 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:18647954 | pubmed:publicationType | Research Support, N.I.H., Intramural | lld:pubmed |
| entrez-gene:27445 | entrezgene:pubmed | pubmed-article:18647954 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:18647954 | lld:entrezgene |
