Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_assertion> ?p ?o ?g. }
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- NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_assertion type Assertion NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_head.
- NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_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." NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.
- NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_assertion evidence source_evidence_literature NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.
- NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_assertion SIO_000772 21266382 NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.
- NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_assertion wasDerivedFrom befree-20150227 NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.
- NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_assertion wasGeneratedBy ECO_0000203 NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.