Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_assertion type Assertion NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_head.
- NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_assertion description "[The natural history of all known patients with French-Canadian Leigh disease (Saguenay-Lac-St-Jean cytochrome c oxidase deficiency, MIM220111, SLSJ-COX), the largest known cohort of patients with a genetically homogeneous, nuclear encoded congenital lactic acidosis, was studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_provenance.
- NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_assertion evidence source_evidence_literature NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_provenance.
- NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_assertion SIO_000772 21266382 NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_provenance.
- NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_assertion wasDerivedFrom befree-2016 NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_provenance.
- NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_assertion wasGeneratedBy ECO_0000203 NP867648.RApyYrfdke-T91rdjqGsq8hhqptqXo3fJc73c98SQfWas130_provenance.