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- source_evidence_literature type ECO_0000212 NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_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." NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_assertion evidence source_evidence_literature NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_assertion SIO_000772 16402916 NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_assertion wasDerivedFrom befree-20150227 NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_assertion wasGeneratedBy ECO_0000203 NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_provenance.