Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- befree-2016 importedOn "2016-02-19" NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_assertion wasGeneratedBy ECO_0000203 NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_assertion wasDerivedFrom befree-2016 NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_assertion SIO_000772 15863660 NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_assertion evidence source_evidence_literature NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.
- NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_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." NP492376.RAZnpJ2UfYgGgDgJ_KSQolt6tmec0zToyTLtpCBTyHxLw130_provenance.