Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_assertion description "[This review focuses on our current understanding of nuclear gene mutations that produce mtDNA alterations and cause mitochondrial depletion syndrome (MDS), progressive external ophthalmoplegia (PEO), ataxia-neuropathy, or mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_assertion evidence source_evidence_literature NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_assertion SIO_000772 17892433 NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_assertion wasDerivedFrom befree-20140225 NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_assertion wasGeneratedBy ECO_0000203 NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP774295.RAYHoKcTUlz5MKxqLULk98y9iQAsZh70iWmLw7Vx32tNU130_provenance.