Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_assertion description "[We screened 230 individuals with primary periodic paralysis for mutations in the SCN4A, CACNA1S, and KCNJ2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_assertion evidence source_evidence_literature NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_assertion SIO_000772 22926674 NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_assertion wasDerivedFrom befree-20140225 NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_assertion wasGeneratedBy ECO_0000203 NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP688706.RAUkOdvFYLILCMWPomzWd1IlFg5dq9T8cgKiWDh2F7Mkc130_provenance.