http://rdf.disgenet.org/resource/nanopub/NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ
type: Nanopublication
created: 2016-05-13T12:46:12+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/NP588738.RA0fYl2Iogxeej67r9jNACZtQI8pU1SL6jcqmBSKmVDGQ130_assertion
type: Assertion
description: [Based on these data, we hypothesize that Cx26 profound hearing loss may be not always congenital, with the possibility of an early window of functional time before the final defect is established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17222463
was generated by: ECO_0000203

befree-2016
imported on: 2016-02-19

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

disgenetv3.0rdf
version: v4.0.0