IDbases are locus-specific databases for immunodeficiency-causing mutations. Our aim is to establish database for every immunodeficiency or provide links to those maintained elsewhere.
|Parent Organization:||University of Tampere; Tampere; Finland|
|Resource Type(s):||Database, Data repository|
|Keywords:||Gene, Clinical, Database, Immunodeficiency, Immunological database, Locus, Mutation, Presentation, Specific|
|Link to OWL / RDF:||Download this content as OWL/RDF|
Curation status: Uncurated
This resource will be curated within 7 days.
For Resource Owners:
After the resource is curated, you may create a sitemap, which will help keep your registry description up-to-date and inform search engines about your resource.
Note: For a new resource, the website's URL must first be verified by a NIF curator before you may proceed.
Learn more about what NIF can do for your resource.
Proudly proclaim your inclusion in NIF by displaying the "Registered with NIF" button on your site. Please login to create the sitemap. (top right)
This page uses this default form:Resource
*Note: Neurolex imports many terms and their ids from existing community ontologies, e.g., the Gene Ontology. Neurolex, however, is a dynamic site and any content beyond the identifier should not be presumed to reflect the content or views of the source ontology. Users should consult with the authoritative source for each ontology for current information.
IDbases are locus-specific databas …
proprietary MUTbase software suite.
|Has default formThis property is a special property in this wiki.||Resource +|
|Has role||Database +, and Data repository +|
|Is part of||University of Tampere; Tampere; Finland +|
|Keywords||Gene +, Clinical +, Database +, Immunodeficiency +, Immunological database +, Locus +, Mutation +, Presentation +, and Specific +|
|ModifiedDate||2 February 2015 +|
|Page has default formThis property is a special property in this wiki.||Resource +|