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- source_evidence_literature type ECO_0000212 NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_assertion description "[Mitochondrial encephalomyopathies are usually divided into three distinct clinical subgroups: (1) mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS); (2) myoclonus epilepsy associated with ragged-red fibres (MERRF); and (3) chronic progressive external ophthalmoplegia (CPEO) including Kearns-Sayre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_assertion evidence source_evidence_literature NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_assertion SIO_000772 2102678 NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_assertion wasDerivedFrom befree-20140225 NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_assertion wasGeneratedBy ECO_0000203 NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP393496.RAmFtPqprd1j05nDaB7qQYCADBk40pz9CbDqlrU-JnO6Q130_provenance.