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期刊名:Journal of biomedical semantics

缩写:J BIOMED SEMANT

ISSN:2041-1480

e-ISSN:2041-1480

IF/分区:2.6/Q2

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共收录本刊相关文章索引569
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Stephen T Wu,Vinod C Kaggal,Dmitriy Dligach et al. Stephen T Wu et al.
Background: One challenge in reusing clinical data stored in electronic medical records is that these data are heterogenous. Clinical Natural Language Processing (NLP) plays an important role in transforming information i...
Charalampos Doulaverakis,George Nikolaidis,Athanasios Kleontas et al. Charalampos Doulaverakis et al.
Background: Identification of drug-drug and drug-diseases interactions can pose a difficult problem to cope with, as the increasingly large number of available drugs coupled with the ongoing research activities in the pha...
Cui Tao,Yongqun He,Hannah Yang et al. Cui Tao et al.
Background: The U.S. FDA/CDC Vaccine Adverse Event Reporting System (VAERS) provides a valuable data source for post-vaccination adverse event analyses. The structured data in the system has been widely used, but the info...
Junguk Hur,Arzucan Ozgür,Zuoshuang Xiang et al. Junguk Hur et al.
Background: Fever is one of the most common adverse events of vaccines. The detailed mechanisms of fever and vaccine-associated gene interaction networks are not fully understood. In the present study, we employed a genom...
Yu Lin,Yongqun He Yu Lin
Background: A vaccine is a processed material that if administered, is able to stimulate an adaptive immune response to prevent or ameliorate a disease. A vaccination process may protect the host against subsequent exposu...
Qian Zhu,Guoqian Jiang,Christopher G Chute Qian Zhu
Background: Structured Product Labeling (SPL) is a document markup standard approved by Health Level Seven (HL7) and adopted by United States Food and Drug Administration (FDA) as a mechanism for exchanging drug product i...
Harsha Gurulingappa,Abdul Mateen-Rajput,Luca Toldo Harsha Gurulingappa
: The sheer amount of information about potential adverse drug events published in medical case reports pose major challenges for drug safety experts to perform timely monitoring. Efficient strategies for identification and extraction of in...
Yongqun He,Luca Toldo,Gully Burns et al. Yongqun He et al.
Vaccines and drugs have contributed to dramatic improvements in public health worldwide. Over the last decade, there have been efforts in developing biomedical ontologies that represent various areas associated with vaccines and drugs. Thes...
Tim Beck,Robert C Free,Gudmundur A Thorisson et al. Tim Beck et al.
Background: The amount of data generated from genome-wide association studies (GWAS) has grown rapidly, but considerations for GWAS phenotype data reuse and interchange have not kept pace. This impacts on the work of GWAS...
Eleni Mikroyannidi,Robert Stevens,Luigi Iannone et al. Eleni Mikroyannidi et al.
Motivation: In this paper we demonstrate the usage of RIO; a framework for detecting syntactic regularities using cluster analysis of the entities in the signature of an ontology. Quality assurance in ontologies is vital ...