Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_assertion description "[We have recently shown, with others, that mutations in the OPA1 gene encoding a dynamin-related mitochondrial protein, underlie the dominant form of optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_assertion evidence source_evidence_literature NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_assertion SIO_000772 11810270 NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_assertion wasDerivedFrom befree-20140225 NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_assertion wasGeneratedBy ECO_0000203 NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP330213.RA4f8pue4JF9nk6Ljy7DWWp5BKrbn5rKsOHLICNEtjGrM130_provenance.