Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_assertion description "[Although all previously reported mutations in the SURF1 gene have been found in patients with cytochrome oxidase (COX)-deficient Leigh syndrome, the phenotype associated with SURF1 protein deficiency should be extended to include leukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_assertion evidence source_evidence_literature NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_assertion SIO_000772 11409433 NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_assertion wasDerivedFrom befree-20140225 NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_assertion wasGeneratedBy ECO_0000203 NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532835.RAwINk-LvHN6SJwEqt0PakGv2Lrpug7a5o-BMNlfKluvQ130_provenance.