| pubmed-article:16755236 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C0029408 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C0016129 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C0003087 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C1384665 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C1384584 | lld:lifeskim |
| pubmed-article:16755236 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
| pubmed-article:16755236 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:16755236 | pubmed:dateCreated | 2006-6-6 | lld:pubmed |
| pubmed-article:16755236 | pubmed:abstractText | Osteoarthritis (OA) can occur in the ankle joint. It also occurs in an appreciable proportion of subjects with hereditary hemochromatosis (HH). Might these conditions have common genetic characteristics? The aim of this study was to test the hypothesis that HFE gene mutations are associated with primary osteoarthritis in the ankle joint. | lld:pubmed |
| pubmed-article:16755236 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16755236 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16755236 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16755236 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16755236 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16755236 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16755236 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16755236 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:16755236 | pubmed:issn | 1076-1608 | lld:pubmed |
| pubmed-article:16755236 | pubmed:author | pubmed-author:CarrollGraeme... | lld:pubmed |
| pubmed-article:16755236 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16755236 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:16755236 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16755236 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16755236 | pubmed:pagination | 109-13 | lld:pubmed |
| pubmed-article:16755236 | pubmed:dateRevised | 2008-4-10 | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:meshHeading | pubmed-meshheading:16755236... | lld:pubmed |
| pubmed-article:16755236 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16755236 | pubmed:articleTitle | Primary osteoarthritis in the ankle joint is associated with finger metacarpophalangeal osteoarthritis and the H63D mutation in the HFE gene: evidence for a hemochromatosis-like polyarticular osteoarthritis phenotype. | lld:pubmed |
| pubmed-article:16755236 | pubmed:affiliation | ArthroCare Pty Ltd., Mount Lawley, Western Australia, Australia. md@arthrocare.com.au | lld:pubmed |
| pubmed-article:16755236 | pubmed:publicationType | Journal Article | lld:pubmed |
| entrez-gene:3077 | entrezgene:pubmed | pubmed-article:16755236 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:16755236 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16755236 | lld:pubmed |
