Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_assertion wasGeneratedBy ECO_0000203 NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_assertion wasDerivedFrom befree-2016 NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_assertion SIO_000772 23030542 NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_assertion evidence source_evidence_literature NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.
- NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_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." NP1017613.RAdv9ZGSzhQe3a69qXc5i33SiP2YOORPCBUhHfA0eKJHI130_provenance.