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Editome Disease Knowledgebase (EDK): a curated knowledgebase of editome-disease associations in human.
Niu, Guangyi; Zou, Dong; Li, Mengwei; Zhang, Yuansheng; Sang, Jian; Xia, Lin; Li, Man; Liu, Lin; Cao, Jiabao; Zhang, Yang; Wang, Pei; Hu, Songnian; Hao, Lili; Zhang, Zhang.
Afiliación
  • Niu G; BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Zou D; CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Li M; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Zhang Y; BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Sang J; CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Xia L; BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Li M; CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Liu L; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Cao J; BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Zhang Y; CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Wang P; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
  • Hu S; BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Hao L; CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100101, China.
  • Zhang Z; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Nucleic Acids Res ; 47(D1): D78-D83, 2019 01 08.
Article en En | MEDLINE | ID: mdl-30357418
ABSTRACT
RNA editing, as an essential co-/post-transcriptional RNA modification type, plays critical roles in many biological processes and involves with a variety of human diseases. Although several databases have been developed to collect RNA editing data in both model and non-model animals, there still lacks a resource integrating associations between editome and human disease. In this study, we present Editome-Disease Knowledgebase (EDK; http//bigd.big.ac.cn/edk), an integrated knowledgebase of RNA editome-disease associations manually curated from published literatures. In the current version, EDK incorporates 61 diseases associated with 248 experimentally validated abnormal editing events located in 32 mRNAs, 16 miRNAs, 1 lncRNA and 11 viruses, and 44 aberrant activities involved with 6 editing enzymes, which together are curated from more than 200 publications. In addition, to facilitate standardization of editome-disease knowledge integration, we propose a data curation model in EDK, factoring an abundance of relevant information to fully capture the context of editome-disease associations. Taken together, EDK is a comprehensive collection of editome-disease associations and bears the great utility in aid of better understanding the RNA editing machinery and complex molecular mechanisms associated with human diseases.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Procesamiento Postranscripcional del ARN / Edición de ARN / Biología Computacional / Predisposición Genética a la Enfermedad / Bases de Datos Genéticas / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Procesamiento Postranscripcional del ARN / Edición de ARN / Biología Computacional / Predisposición Genética a la Enfermedad / Bases de Datos Genéticas / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2019 Tipo del documento: Article País de afiliación: China