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pubmed-article:16243813 | lifeskim:mentions | umls-concept:C0059563 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C1176140 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C1413882 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C1285572 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C1314763 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C0182400 | lld:lifeskim |
pubmed-article:16243813 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
pubmed-article:16243813 | pubmed:issue | 20 | lld:pubmed |
pubmed-article:16243813 | pubmed:dateCreated | 2005-10-24 | lld:pubmed |
pubmed-article:16243813 | pubmed:abstractText | To evaluate the effect of naturally occurring variants in genes encoding the cytochrome P450 (CYP) isoforms CYP3A4 and CYP3A5 in patients with cancer receiving midazolam as a phenotyping probe. | lld:pubmed |
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pubmed-article:16243813 | pubmed:language | eng | lld:pubmed |
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pubmed-article:16243813 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:16243813 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16243813 | pubmed:month | Oct | lld:pubmed |
pubmed-article:16243813 | pubmed:issn | 1078-0432 | lld:pubmed |
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pubmed-article:16243813 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16243813 | pubmed:day | 15 | lld:pubmed |
pubmed-article:16243813 | pubmed:volume | 11 | lld:pubmed |
pubmed-article:16243813 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16243813 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16243813 | pubmed:pagination | 7398-404 | lld:pubmed |
pubmed-article:16243813 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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pubmed-article:16243813 | pubmed:year | 2005 | lld:pubmed |
pubmed-article:16243813 | pubmed:articleTitle | Effect of common CYP3A4 and CYP3A5 variants on the pharmacokinetics of the cytochrome P450 3A phenotyping probe midazolam in cancer patients. | lld:pubmed |
pubmed-article:16243813 | pubmed:affiliation | Science Applications International Corporation-Frederick, Maryland, USA. | lld:pubmed |
pubmed-article:16243813 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16243813 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:16243813 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:16243813 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:16243813 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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