| pubmed-article:16204165 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C0033137 | lld:lifeskim |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C1527272 | lld:lifeskim |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C0392514 | lld:lifeskim |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C1277709 | lld:lifeskim |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C0696113 | lld:lifeskim |
| pubmed-article:16204165 | lifeskim:mentions | umls-concept:C1955832 | lld:lifeskim |
| pubmed-article:16204165 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:16204165 | pubmed:dateCreated | 2005-10-5 | lld:pubmed |
| pubmed-article:16204165 | pubmed:abstractText | Therapeutic phlebotomy for hereditary hemochromatosis is relatively safe and presumably efficacious when offered before cirrhosis develops, so screening primary care patients is of substantial interest. | lld:pubmed |
| pubmed-article:16204165 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16204165 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:16204165 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:16204165 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16204165 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:16204165 | pubmed:issn | 1539-3704 | lld:pubmed |
| pubmed-article:16204165 | pubmed:author | pubmed-author:GreenRichardR | lld:pubmed |
| pubmed-article:16204165 | pubmed:author | pubmed-author:SchmittBrianB | lld:pubmed |
| pubmed-article:16204165 | pubmed:author | pubmed-author:GolubRobert... | lld:pubmed |
| pubmed-article:16204165 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:16204165 | pubmed:day | 4 | lld:pubmed |
| pubmed-article:16204165 | pubmed:volume | 143 | lld:pubmed |
| pubmed-article:16204165 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16204165 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16204165 | pubmed:pagination | 522-36 | lld:pubmed |
| pubmed-article:16204165 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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| pubmed-article:16204165 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:16204165 | pubmed:articleTitle | Screening primary care patients for hereditary hemochromatosis with transferrin saturation and serum ferritin level: systematic review for the American College of Physicians. | lld:pubmed |
| pubmed-article:16204165 | pubmed:affiliation | Loyola University Medical Center, Maywood, Illinois, USA. brian.schmitt2@med.va.gov | lld:pubmed |
| pubmed-article:16204165 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16204165 | pubmed:publicationType | Review | lld:pubmed |
| pubmed-article:16204165 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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