http://rdf.disgenet.org/resource/nanopub/NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg
type: Nanopublication
created: 2016-05-13T12:52:12+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/NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_assertion
type: Assertion
description: [ROCA, which in southern African Blacks is caused by mutations in the TYRP1 gene, therefore should be referred to as OCA3, since this is the third locus that has been shown to cause an OCA phenotype in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/9345097
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