Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_assertion description "[We sequenced the encoded complex I units: ND2, ND3, ND4, ND5 and ND6 genes and the mitochondrial ATPase 6, tRNA(Val), tRNA(Leu(UUR)), tRNA(Trp) and tRNA(Lys) genes in 10 unrelated patients with Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_assertion evidence source_evidence_literature NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_assertion SIO_000772 19349200 NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_assertion wasDerivedFrom befree-20140225 NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_assertion wasGeneratedBy ECO_0000203 NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP551513.RAlZKPOMTUESnBQDTHKpbHYP4BzIAnMmHMNAqRJ-lHyQk130_provenance.