Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_assertion description "[Point mutations in mitochondrial tRNAs can cause severe multisystemic disorders such as mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) and myoclonus epilepsy with ragged-red fibers (MERRF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_assertion evidence source_evidence_literature NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_assertion SIO_000772 15019775 NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_assertion wasDerivedFrom befree-20140225 NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_assertion wasGeneratedBy ECO_0000203 NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453292.RA2UANS9LuwvbPP--nMn0rIQLeRge9KS2XhxBc4gKAJXI130_provenance.