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- NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_assertion type Assertion NP870374.RAVPshtJS7VBWz6zk-56xao0VzlMqxP5pWLyJ9SB366m4130_head.
- 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.