Skip to main content
Top
Published in: Orphanet Journal of Rare Diseases 2/2012

Open Access 01-11-2012 | Meeting abstract

Speeding up research with the Semantic Web

Authors: Marco Roos, Erik A Schultes, Barend Mons

Published in: Orphanet Journal of Rare Diseases | Special Issue 2/2012

Login to get access

Excerpt

Data for Rare Diseases are often distributed. Ideally, we can combine relevant data and biological insights from any place in the world and use it directly as input for computational analysis. However, too often data is poorly described making it hard to find, hard to assess its quality, and hard to integrate with other data. A valid question is: 'Why can't we analyse data as if it came from one global database?'. Here we introduce the Semantic Web as an enabling technology for making data interoperable and thereby expediting biological insight. …
Metadata
Title
Speeding up research with the Semantic Web
Authors
Marco Roos
Erik A Schultes
Barend Mons
Publication date
01-11-2012
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue Special Issue 2/2012
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-7-S2-A11

Other articles of this Special Issue 2/2012

Orphanet Journal of Rare Diseases 2/2012 Go to the issue

Meeting abstract

Exon skipping for DMD