Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_assertion description "[In the present study we show that the function of the F1F0-ATPase is impaired in lymphocytes from ten individuals harbouring the mtDNA T8993G point mutation associated with NARP (neuropathy, ataxia and retinitis pigmentosa) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_assertion evidence source_evidence_literature NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_assertion SIO_000772 16402916 NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_assertion wasDerivedFrom befree-2016 NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_assertion wasGeneratedBy ECO_0000203 NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.
- befree-2016 importedOn "2016-02-19" NP530271.RA24D7hv2nIB9qGo-oSFmmIa0TWV3E8WWFxQIpcf5nUOk130_provenance.