Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_assertion description "[Familial cortical myoclonus with a mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_assertion evidence source_evidence_curated NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_assertion SIO_000772 22926851 NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_assertion wasDerivedFrom uniprot-2016 NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_assertion wasGeneratedBy ECO_0000218 NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7193.RAlMAa_O2et40q3BhL3Rbd8-xdRIlTgUdboge1Fi7UpMU130_provenance.