| pubmed-article:11087882 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11087882 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:11087882 | lifeskim:mentions | umls-concept:C0080103 | lld:lifeskim |
| pubmed-article:11087882 | lifeskim:mentions | umls-concept:C0018995 | lld:lifeskim |
| pubmed-article:11087882 | lifeskim:mentions | umls-concept:C0348080 | lld:lifeskim |
| pubmed-article:11087882 | pubmed:issue | 21 | lld:pubmed |
| pubmed-article:11087882 | pubmed:dateCreated | 2000-11-8 | lld:pubmed |
| pubmed-article:11087882 | pubmed:abstractText | Hemochromatosis occurs in approximately 5 white people per 1000 and is usually due to homozygosity for mutations in the HLA-linked HFE gene. Although screening has been proposed, the proportion of homozygotes with conditions related to hemochromatosis is uncertain. | lld:pubmed |
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| pubmed-article:11087882 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11087882 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11087882 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11087882 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:11087882 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11087882 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:11087882 | pubmed:issn | 0028-4793 | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:PhillipsJ DJD | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:KushnerJ PJP | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:EdwardsC QCQ | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:JordeL BLB | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:GriffenL MLM | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:AjiokaR SRS | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:LaSalleB ABA | lld:pubmed |
| pubmed-article:11087882 | pubmed:author | pubmed-author:BulajZ JZJ | lld:pubmed |
| pubmed-article:11087882 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11087882 | pubmed:day | 23 | lld:pubmed |
| pubmed-article:11087882 | pubmed:volume | 343 | lld:pubmed |
| pubmed-article:11087882 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11087882 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11087882 | pubmed:pagination | 1529-35 | lld:pubmed |
| pubmed-article:11087882 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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| pubmed-article:11087882 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:11087882 | pubmed:articleTitle | Disease-related conditions in relatives of patients with hemochromatosis. | lld:pubmed |
| pubmed-article:11087882 | pubmed:affiliation | Department of Medicine, University of Utah School of Medicine, Salt Lake City, USA. | lld:pubmed |
| pubmed-article:11087882 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11087882 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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