Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion wasGeneratedBy ECO_0000203 NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion wasDerivedFrom befree-20140225 NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion SIO_000772 10556303 NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion evidence source_evidence_literature NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion description "[Leigh syndrome (LS) associated with cytochrome c oxidase (COX) deficiency is an autosomal recessive neurodegenerative disorder caused by mutations in SURF1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.