Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion> ?p ?o ?g. }
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- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion type Assertion NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_head.
- 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.
- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion evidence source_evidence_literature 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 wasDerivedFrom befree-20140225 NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.
- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion wasGeneratedBy ECO_0000203 NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.