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- source_evidence_literature type ECO_0000212 NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_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." NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_assertion evidence source_evidence_literature NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_assertion SIO_000772 21266382 NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_assertion wasDerivedFrom befree-2016 NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_assertion wasGeneratedBy ECO_0000203 NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.
- befree-2016 importedOn "2016-02-19" NP867656.RAMENiOHL5F5igoyEpdpgrN2FlVFRbRob2KRn515n28UE130_provenance.