Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_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." NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_assertion evidence source_evidence_literature NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_assertion SIO_000772 16402916 NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_assertion wasDerivedFrom befree-20140225 NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_assertion wasGeneratedBy ECO_0000203 NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP450982.RASesBjTti5BO8bcXd2pwy2JeHcChS9epq1-jrl-xv0MI130_provenance.