12792018

Source:http://linkedlifedata.com/resource/pubmed/id/12792018

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220905, umls-concept:C0546881, umls-concept:C0680240, umls-concept:C1705413, umls-concept:C2607850
pubmed:issue	3
pubmed:dateCreated	2003-6-6
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101136980
pubmed:citationSubset	H
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1475-3898
pubmed:author	pubmed-author:DebanneS MSM, pubmed-author:NeuhauserDD, pubmed-author:SantiagoL MLM
pubmed:issnType	Print
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	234-5
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:12792018-Adverse Drug Reaction Reporting Systems, pubmed-meshheading:12792018-Government Agencies, pubmed-meshheading:12792018-Humans, pubmed-meshheading:12792018-National Institutes of Health (U.S.), pubmed-meshheading:12792018-Randomized Controlled Trials as Topic, pubmed-meshheading:12792018-United States
pubmed:year	2003
pubmed:articleTitle	Tracking adverse events in RCTs: lack of agreement among regulatory institutions.
pubmed:publicationType	Letter