Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_assertion wasGeneratedBy ECO_0000203 NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_assertion wasDerivedFrom befree-20140225 NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_assertion SIO_000772 23030542 NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_assertion evidence source_evidence_literature NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_assertion description "[Genetic studies in the rare form of familial hemiplegic migraine have identified mutations in 3 genes (CACNA1A, ATP1A2, and SCN1A) encoding proteins involved in ion homeostasis and suggesting that other such genes may be involved in the more common forms of migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP866277.RAbyeA2DdJvbHvXcGwLkENO0bDm3A8iDNjCHRYe6UeBaA130_provenance.