Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_assertion description "[Defects in NADH:ubiquinone oxidoreductase, the complex I of the mitochondrial respiratory chain represents the most frequent cause of mitochondrial diseases and is associated with a wide clinical spectrum varying from severe lactic acidosis in infants to muscle weakness in adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_assertion evidence source_evidence_literature NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_assertion SIO_000772 17275378 NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_assertion wasDerivedFrom befree-20150227 NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_assertion wasGeneratedBy ECO_0000203 NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.
- befree-20150227 importedOn "2015-02-27" NP800025.RAKNzWLo_lmEeBXGQcZoeaW8Rhf-xyM5w8EEVr4zClHms130_provenance.