http://rdf.disgenet.org/resource/nanopub/NP205914.RAcYQzXUAaQYUxs1uzKnmRuX3GbTmS3Kl-EG6Fejc418M
type: Nanopublication
created: 2016-05-13T12:43:20+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetv3.0rdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v4.0.0.0

http://rdf.disgenet.org/resource/nanopub/NP205914.RAcYQzXUAaQYUxs1uzKnmRuX3GbTmS3Kl-EG6Fejc418M130_assertion
type: Assertion
description: [mutations in the WT1 have been found to be present in patients with SRNS in association with Wilms'tumor (WT) and urinary or genital malformations, as well as in patients with isolated steroid resistant nephrotic syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15253707
was generated by: ECO_0000203

lhgdn-20090331
imported on: 2009-03-31

DisGeNET evidence - LITERATURE
type: ECO_0000212
comment: Gene-disease associations inferred from text-mining the literature.

disgenetv3.0rdf
version: v4.0.0