http://rdf.disgenet.org/resource/nanopub/NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw
type: Nanopublication
created: 2016-05-13T12:43:24+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/NP215335.RAHxTPli_IsUuYNc9hUngcxhG9Xq0imHSH2EnU_fVCjFw130_assertion
type: Assertion
description: [Acquisition of the wobble modification in another isoacceptor tRNA is critical for suppressing the MELAS mutation, highlighting the primary role of the UUG decoding deficiency in the molecular pathogenesis of MELAS syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/16446307
was generated by: ECO_0000203

lhgdn-20090331
imported on: 2009-03-31

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

disgenetv3.0rdf
version: v4.0.0