Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion wasGeneratedBy ECO_0000203 NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion wasDerivedFrom befree-20150227 NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion SIO_000772 15863660 NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion evidence source_evidence_literature NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion description "[Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.