Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_assertion type Assertion NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_head.
- NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_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." NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_provenance.
- NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_assertion evidence source_evidence_literature NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_provenance.
- NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_assertion SIO_000772 16402916 NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_provenance.
- NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_assertion wasDerivedFrom befree-20150227 NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_provenance.
- NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_assertion wasGeneratedBy ECO_0000203 NP870387.RAd85LpPSHz_1r0Ng1D9xfk8MgxIYHmfvYMaLoNMxz7PU130_provenance.