Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP821965.RAIo4OvS14A2cXxTpCda3NyACWpkDK3sNOZBWneP86U_M130_provenance.