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- source_evidence_literature type ECO_0000212 NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_assertion description "[Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_assertion evidence source_evidence_literature NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_assertion SIO_000772 16645216 NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_assertion wasDerivedFrom befree-2016 NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_assertion wasGeneratedBy ECO_0000203 NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.
- befree-2016 importedOn "2016-02-19" NP547280.RATw8u6Q9_OCe3b9yV8gFbn4ugCmCFSvA4C0qNc-GTGSo130_provenance.