| pubmed-article:17916170 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17916170 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:17916170 | lifeskim:mentions | umls-concept:C0014507 | lld:lifeskim |
| pubmed-article:17916170 | lifeskim:mentions | umls-concept:C2711227 | lld:lifeskim |
| pubmed-article:17916170 | lifeskim:mentions | umls-concept:C1384665 | lld:lifeskim |
| pubmed-article:17916170 | lifeskim:mentions | umls-concept:C0151763 | lld:lifeskim |
| pubmed-article:17916170 | lifeskim:mentions | umls-concept:C0178555 | lld:lifeskim |
| pubmed-article:17916170 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:17916170 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:17916170 | pubmed:dateCreated | 2008-4-2 | lld:pubmed |
| pubmed-article:17916170 | pubmed:abstractText | The altered status of iron metabolism is reported in hereditary haemochromatosis and in non-alcoholic liver fatty disease. We investigated the relation between the H63D HFE mutation gene and non-alcoholic steatohepatitis (NASH). | lld:pubmed |
| pubmed-article:17916170 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17916170 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17916170 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17916170 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17916170 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17916170 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17916170 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17916170 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:17916170 | pubmed:issn | 1445-5994 | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:SignorelliSS | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:NeriSS | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:CastellinoPP | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:CutuliNN | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:PulvirentiDD | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:URONEP FPF | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:MauceriBB | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:IgnaccoloLL | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:MisseriMM | lld:pubmed |
| pubmed-article:17916170 | pubmed:author | pubmed-author:InterlandiDD | lld:pubmed |
| pubmed-article:17916170 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:17916170 | pubmed:volume | 38 | lld:pubmed |
| pubmed-article:17916170 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17916170 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17916170 | pubmed:pagination | 254-8 | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:meshHeading | pubmed-meshheading:17916170... | lld:pubmed |
| pubmed-article:17916170 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:17916170 | pubmed:articleTitle | The HFE gene heterozygosis H63D: a cofactor for liver damage in patients with steatohepatitis? Epidemiological and clinical considerations. | lld:pubmed |
| pubmed-article:17916170 | pubmed:affiliation | Department of Internal Medicine and Systemic Diseases, Policlinic of Catania University, Catania, Italy. sergio.neri4@tin.it <sergio.neri4@tin.it> | lld:pubmed |
| pubmed-article:17916170 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17916170 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:3077 | entrezgene:pubmed | pubmed-article:17916170 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:17916170 | lld:entrezgene |
