Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_assertion description "[Nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase (complex I) enzyme deficiencies account for a significant proportion of mitochondrial disorders, including LS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_assertion evidence source_evidence_literature NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_assertion SIO_000772 23266820 NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_assertion wasDerivedFrom befree-20140225 NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_assertion wasGeneratedBy ECO_0000203 NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP388127.RARHIQTwq5-9hzXoVjyklzJ0jeIwD6hbIdnPyxoGhr0fc130_provenance.