Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_assertion> ?p ?o ?g. }
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- NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_assertion type Assertion NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_head.
- NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_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." NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_provenance.
- NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_assertion evidence source_evidence_literature NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_provenance.
- NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_assertion SIO_000772 21266382 NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_provenance.
- NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_assertion wasDerivedFrom befree-20140225 NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_provenance.
- NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_assertion wasGeneratedBy ECO_0000203 NP699191.RAVrBNC2hmDWVSZ07yNEezI273Gcmh2NqnJL-Qfa4FWb4130_provenance.