DisGeNET-RDF: harnessing the innovative power of the Semantic Web to explore the genetic basis of diseases
about
DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variantsGenome-wide analysis of differential RNA editing in epilepsy.Open PHACTS computational protocols for in silico target validation of cellular phenotypic screens: knowing the knowns.Reliable Granular References to Changing Linked DataGenomic determinants of long-term cardiometabolic complications in childhood acute lymphoblastic leukemia survivors.Links between critical proteins drive the controllability of protein interaction networks.What incentives increase data sharing in health and medical research? A systematic review.A TRPV2 interactome-based signature for prognosis in glioblastoma patients.Gene's hubs in retinal diseases: A retinal disease network
P2860
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P2860
DisGeNET-RDF: harnessing the innovative power of the Semantic Web to explore the genetic basis of diseases
description
2016 nî lūn-bûn
@nan
2016 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@ast
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@en
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@nl
type
label
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@ast
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@en
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@nl
prefLabel
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@ast
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@en
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@nl
P2860
P50
P921
P3181
P356
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P1476
DisGeNET-RDF: harnessing the i ...... the genetic basis of diseases
@en
P2093
Àlex Bravo
P2860
P304
P3181
P356
10.1093/BIOINFORMATICS/BTW214
P407
P577
2016-07-15T00:00:00Z