Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_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." NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_assertion evidence source_evidence_literature NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_assertion SIO_000772 16402916 NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_assertion wasDerivedFrom befree-20150227 NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_assertion wasGeneratedBy ECO_0000203 NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP598301.RAyfiHeHloWd5z_8rGB3I-i_iLArkZPCTdtjynu11IwjU130_provenance.