http://rdf.disgenet.org/resource/nanopub/NP15831.RAERZXvEBbukK-rm06z5Ctlc6CqzSIIxCmIqpaPhrRzWY
type: Nanopublication
created: 2016-05-13T12:41:56+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/NP15831.RAERZXvEBbukK-rm06z5Ctlc6CqzSIIxCmIqpaPhrRzWY130_assertion
type: Assertion
description: [We studied 11 individuals with renal tubular dysgenesis, belonging to nine families, and found that they had homozygous or compound heterozygous mutations in the genes encoding renin, angiotensinogen, angiotensin converting enzyme or angiotensin II receptor type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - CURATED
SIO_000772: http://identifiers.org/pubmed/16116425
was generated by: ECO_0000218

ctd human-2016
imported on: 2016-01-25

DisGeNET evidence - CURATED
type: ECO_0000205
comment: Gene-disease associations manually curated.

disgenetv3.0rdf
version: v4.0.0