Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_assertion> ?p ?o ?g. }
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- NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_assertion type Assertion NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_head.
- NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_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." NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_provenance.
- NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_assertion evidence source_evidence_literature NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_provenance.
- NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_assertion SIO_000772 16402916 NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_provenance.
- NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_assertion wasDerivedFrom befree-2016 NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_provenance.
- NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_assertion wasGeneratedBy ECO_0000203 NP530274.RAj_EvOgtd0ENCUTqj-VB62LotTVpcBcyycWXpDCor6No130_provenance.