Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_assertion description "[Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_assertion evidence source_evidence_literature NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_assertion SIO_000772 16402916 NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_assertion wasDerivedFrom befree-2016 NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_assertion wasGeneratedBy ECO_0000203 NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.
- befree-2016 importedOn "2016-02-19" NP530272.RAiUOanAGeYAt1g6iHSTfo0IXlAMfEZvCiryJVURijXRc130_provenance.