pubmed-article:20145272 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C1556084 | lld:lifeskim |
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pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0017431 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0314603 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0033105 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0524899 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0034975 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0336791 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:20145272 | lifeskim:mentions | umls-concept:C1710133 | lld:lifeskim |
pubmed-article:20145272 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:20145272 | pubmed:dateCreated | 2010-4-9 | lld:pubmed |
pubmed-article:20145272 | pubmed:abstractText | Despite great progress in understanding the mechanisms underlying genetic hemochromatosis, data on the prevalence and the penetrance of the disorder are conflicting. | lld:pubmed |
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pubmed-article:20145272 | pubmed:language | eng | lld:pubmed |
pubmed-article:20145272 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20145272 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20145272 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20145272 | pubmed:month | Apr | lld:pubmed |
pubmed-article:20145272 | pubmed:issn | 1592-8721 | lld:pubmed |
pubmed-article:20145272 | pubmed:author | pubmed-author:JorgensenChri... | lld:pubmed |
pubmed-article:20145272 | pubmed:author | pubmed-author:Giansily-Blai... | lld:pubmed |
pubmed-article:20145272 | pubmed:author | pubmed-author:Aguilar-Marti... | lld:pubmed |
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pubmed-article:20145272 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20145272 | pubmed:volume | 95 | lld:pubmed |
pubmed-article:20145272 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20145272 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20145272 | pubmed:pagination | 551-6 | lld:pubmed |
pubmed-article:20145272 | pubmed:dateRevised | 2010-9-27 | lld:pubmed |
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pubmed-article:20145272 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20145272 | pubmed:articleTitle | The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance. | lld:pubmed |
pubmed-article:20145272 | pubmed:affiliation | CHU of Montpellier Laboratory of Hematology, Hôpital Saint Eloi, Avenue Augustin Fliche, 34295 Montpellier Cedex 5, France. p-martinez@chu-montpellier.fr | lld:pubmed |
pubmed-article:20145272 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20145272 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:20145272 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:3077 | entrezgene:pubmed | pubmed-article:20145272 | lld:entrezgene |
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