http://rdf.disgenet.org/nanopublications.trig#NP735.RAGZ8TSNceLwuWne5OOzXlnfPJss5a2Q791--7LoMjoxk
type: Nanopublication
created: 2014-10-02T12:31:58+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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: v2.1.0.0

http://rdf.disgenet.org/nanopublications.trig#NP735.RAGZ8TSNceLwuWne5OOzXlnfPJss5a2Q791--7LoMjoxk130_assertion
type: Assertion
description: [Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - CURATED
SIO_000772: http://identifiers.org/pubmed/21922595
was generated by: ECO_0000218

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

uniprot-20130724
imported on: 2013-07-24

disgenetrdf
version: v2.1.0