Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_assertion description "[Homozygosity mapping of 5 patients from a consanguineous family with infantile mitochondrial encephalomyopathy resulted in the identification of a missense mutation in a conserved residue of the C6ORF66.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_assertion evidence source_evidence_literature NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_assertion SIO_000772 18179882 NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_assertion wasDerivedFrom lhgdn-20090331 NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_assertion wasGeneratedBy ECO_0000203 NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP146696.RAa9ALgi95MyvGXcxAq5eLuQOdCZqr9K_ritAcGl9lXM8130_provenance.