Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_assertion description "[The Leigh syndrome of SLSJ-COX differs from that of SURF1-related COX deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_assertion evidence source_evidence_literature NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_assertion SIO_000772 21266382 NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_assertion wasDerivedFrom befree-20140225 NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_assertion wasGeneratedBy ECO_0000203 NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP294124.RA9Kr2GxNrfVxHQHK6o1PWHWLvN6ZkytmZXXrjjre0AgE130_provenance.