http://rdf.disgenet.org/resource/nanopub/NP62298.RA2og7jYVJaRZq9clWap_m-mV2jGUZYdhT_hbVrsJpT1c
type: Nanopublication
created: 2016-05-13T12:42:16+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/NP62298.RA2og7jYVJaRZq9clWap_m-mV2jGUZYdhT_hbVrsJpT1c130_assertion
type: Assertion
description: [Our data suggest that hepatic cystogenesis in autosomal recessive polycystic kidney disease may involve increased fluid accumulation because of overexpression and abnormal location of AQP1, CFTR, and AE2 in cystic cholangiocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - PREDICTED
SIO_000772: http://identifiers.org/pubmed/18988797
was generated by: ECO_0000218

rgd-2016
imported on: 2016-01-25

DisGeNET evidence - PREDICTED
type: ECO_0000266
comment: Gene-disease associations inferred from animal model manually asserted gene-disease associations.

disgenetv3.0rdf
version: v4.0.0