Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_assertion description "[Mutations in CACNA1A encoding a neuronal calcium channel and ATP1A2 encoding an ion pump cause episodic ataxia, hemiplegic migraine, and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_assertion evidence source_evidence_literature NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_assertion SIO_000772 16116111 NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_assertion wasDerivedFrom befree-20140225 NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_assertion wasGeneratedBy ECO_0000203 NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP800722.RA_oI6Y4279fwUwlUwR9aFYgg_cSYmFBL1n6GYA3SdaeE130_provenance.