| pubmed-article:15730420 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15730420 | lifeskim:mentions | umls-concept:C0018213 | lld:lifeskim |
| pubmed-article:15730420 | lifeskim:mentions | umls-concept:C0009221 | lld:lifeskim |
| pubmed-article:15730420 | lifeskim:mentions | umls-concept:C0025646 | lld:lifeskim |
| pubmed-article:15730420 | lifeskim:mentions | umls-concept:C0042285 | lld:lifeskim |
| pubmed-article:15730420 | lifeskim:mentions | umls-concept:C1539897 | lld:lifeskim |
| pubmed-article:15730420 | lifeskim:mentions | umls-concept:C0004083 | lld:lifeskim |
| pubmed-article:15730420 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:15730420 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:15730420 | pubmed:dateCreated | 2005-2-25 | lld:pubmed |
| pubmed-article:15730420 | pubmed:abstractText | A functional polymorphism at codon 55 of the small ubiquitin-like modifier-4 (SUMO4) gene (methionine to valine; M55V) has recently been associated with type 1 diabetes mellitus (T1D). We aimed to establish whether this locus also contributes towards the genetic susceptibility to Graves' disease (GD) and autoimmune Addison's disease. | lld:pubmed |
| pubmed-article:15730420 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15730420 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15730420 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15730420 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15730420 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15730420 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15730420 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15730420 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15730420 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15730420 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:15730420 | pubmed:issn | 0300-0664 | lld:pubmed |
| pubmed-article:15730420 | pubmed:author | pubmed-author:WilsonValerie... | lld:pubmed |
| pubmed-article:15730420 | pubmed:author | pubmed-author:PearceSimon... | lld:pubmed |
| pubmed-article:15730420 | pubmed:author | pubmed-author:JenningsClair... | lld:pubmed |
| pubmed-article:15730420 | pubmed:author | pubmed-author:OwenCatherine... | lld:pubmed |
| pubmed-article:15730420 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15730420 | pubmed:volume | 62 | lld:pubmed |
| pubmed-article:15730420 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15730420 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15730420 | pubmed:pagination | 362-5 | lld:pubmed |
| pubmed-article:15730420 | pubmed:dateRevised | 2005-11-17 | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:meshHeading | pubmed-meshheading:15730420... | lld:pubmed |
| pubmed-article:15730420 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15730420 | pubmed:articleTitle | No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves' disease. | lld:pubmed |
| pubmed-article:15730420 | pubmed:affiliation | Institute of Human Genetics and School of Clinical Medical Sciences, University of Newcastle, Newcastle upon Tyne, UK. | lld:pubmed |
| pubmed-article:15730420 | pubmed:publicationType | Journal Article | lld:pubmed |
| entrez-gene:387082 | entrezgene:pubmed | pubmed-article:15730420 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:15730420 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15730420 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15730420 | lld:pubmed |
