Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_assertion description "[ATP1A3 mutation analysis is appropriate to consider in the diagnostic algorithm for any child presenting with episodic or fluctuating ataxia, weakness or dystonia whether they manifest persistence of neurological symptoms between episodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_assertion evidence source_evidence_literature NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_assertion SIO_000772 25447930 NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_assertion wasDerivedFrom befree-2016 NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_assertion wasGeneratedBy ECO_0000203 NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1242286.RADBp7GjeRfBLKOaBhnK-WCgFXM2E97mfGPJKzeacrTwM130_provenance.