{"prefix":"fsnp","name":"F-SNP","description":"The Functional Single Nucleotide Polymorphism (F-SNP) database integrates information obtained from databases about the functional effects of SNPs. These effects are predicted and indicated at the splicing, transcriptional, translational and post-translational level. In particular, users can retrieve SNPs that disrupt genomic regions known to be functional, including splice sites and transcriptional regulatory regions. Users can also identify non-synonymous SNPs that may have deleterious effects on protein structure or function, interfere with protein translation or impede post-translational modification.","pattern":"^rs\\d+$","uri_format":"http://compbio.cs.queensu.ca/cgi-bin/compbio/search/main.cgi?search_mode=id&id_type=snp_id&id_val=$1","providers":[{"code":"bio2rdf","name":"Bio2RDF","description":"Bio2RDF is an open-source project that uses Semantic Web technologies to build and provide the largest network of Linked Data for the Life Sciences. Bio2RDF defines a set of simple conventions to create RDF(S) compatible Linked Data from a diverse set of heterogeneously formatted sources obtained from multiple data providers.","homepage":"https://bio2rdf.org","uri_format":"http://bio2rdf.org/fsnp:$1"}],"homepage":"http://compbio.cs.queensu.ca/F-SNP/","example":"rs17852708","example_extras":[],"deprecated":true,"mappings":{"biocontext":"FSNP","miriam":"fsnp","n2t":"fsnp","prefixcommons":"fsnp"},"synonyms":[],"keywords":["dna","protein"],"publications":[],"appears_in":[],"depends_on":[],"namespace_in_lui":false,"preferred_prefix":"fsnp"}