Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_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." NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_assertion evidence source_evidence_literature NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_assertion SIO_000772 16402916 NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_assertion wasDerivedFrom befree-20140225 NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_assertion wasGeneratedBy ECO_0000203 NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718898.RAHsTorXP6LXVFIexNOTzdL-MPhveZYc4XCTEQT5NuhXI130_provenance.