Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_assertion description "[We hypothesized that mutations in SCARB2 might account for unsolved cases of progressive myoclonus epilepsy (PME) without renal impairment, especially those resembling Unverricht-Lundborg disease (ULD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_assertion evidence source_evidence_literature NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_assertion SIO_000772 19847901 NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_assertion wasDerivedFrom befree-20140225 NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_assertion wasGeneratedBy ECO_0000203 NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP429649.RAZIE0wxTVdYiQ10nCkiJ8uZ2Wkq3L8heptD3h-bJncG4130_provenance.