Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_assertion description "[Skeletal muscle dihydropyridine-sensitive calcium channel (CACNA1S) gene mutations in chinese patients with hypokalemic periodic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_assertion evidence source_evidence_literature NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_assertion SIO_000772 15711422 NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_assertion wasDerivedFrom befree-20140225 NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_assertion wasGeneratedBy ECO_0000203 NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP188155.RANOE6TNfwl-4Yg8PWidc9_apLm2Pn9HTozK-hzAg5J7c130_provenance.