All association data in ncRNAVar can be freely download for academic purposes.
|ncRNA variation-disease phenotype association.txt||The core association data in ncRNAVar, including association ID, ncRNA symbol, ncRNA type, variation, ontology ID, disease phenotype, association score, allel, chromosome position, comma delimited list of allele frequencies based on 1000Genomes and TOPMED, SNP position, GWAVA-Score, CADD-Score etc.|
|ncRNA information.txt||The detailed data of ncRNAs, including ncRNA symbol, category, NCBI geneID, miRBase ID, piRBase ID, NONCODE ID, alias, etc.|
|Disease phenotype information.txt||The detailed data of disease phenotypes, including disease phenotype, ontology ID, disease phenotype name, definition, alterative name, cross reference, etc.|
|Evidence information in publications.txt||The detailed data in publications for supporting the associations, including association ID, PMID, ncRNA, variation, risk allele, inheritance model, sample size, disease phenotype ontology ID, treatment, clinical significance, disease phenotype, supporting evidence description and association score.|