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Standardizing adverse drug event reporting data

BACKGROUND: The Adverse Event Reporting System (AERS) is an FDA database providing rich information on voluntary reports of adverse drug events (ADEs). Normalizing data in the AERS would improve the mining capacity of the AERS for drug safety signal detection and promote semantic interoperability be...

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Sonraí Bibleagrafaíochta
Main Authors: Wang, Liwei, Jiang, Guoqian, Li, Dingcheng, Liu, Hongfang
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2014
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4142531/
https://ncbi.nlm.nih.gov/pubmed/25157320
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2041-1480-5-36
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