DISNOR

This FAIRsharing record describes: DISNOR is a resource that uses a comprehensive collection of disease associated genes, as annotated in DisGeNET, to interrogate SIGNOR (https://signor.uniroma2.it) in order to assemble disease-specific logic networks linking disease associated genes by causal relationships. DISNOR is an open resource where more than 4000 disease-networks, linking ~ 2800 disease genes, can be explored. For each disease curated in DisGeNET, DISNOR links disease genes through manually annotated causal relationships and the inferred 'patho-pathways' can be visualised at different level of complexity.本FAIRsharing记录所介绍的内容如下：DISNOR是一款基于DisGeNET注释的全面疾病关联基因集合，对SIGNOR（https://signor.uniroma2.it）开展检索分析，以构建通过因果关系连接疾病关联基因的疾病特异性逻辑网络的开源资源。该资源包含超过4000个疾病网络，连接约2800个疾病基因，可供用户探索分析。针对DisGeNET中经人工整理注释的每一种疾病，DISNOR均通过人工注释的因果关系连接其关联疾病基因，且所推断得到的病理通路可按不同复杂程度进行可视化展示。

搜集汇总

背景与挑战

背景概述

DISNOR是一个疾病网络开放资源，利用DisGeNET注释的疾病相关基因集合，构建疾病特异性逻辑网络，链接约2800个基因，并提供可视化功能。该资源自2016年创建，由意大利的研究机构维护，覆盖生命科学和生物医学领域。