Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_assertion description "[Interest in ion channels in migraine has been spurred by molecular genetic findings in familial hemiplegic migraine, since familial hemiplegic migraine type 1 is caused by mutations in the calcium channel gene CACNA1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_assertion evidence source_evidence_literature NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_assertion SIO_000772 15705118 NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_assertion wasDerivedFrom befree-20140225 NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_assertion wasGeneratedBy ECO_0000203 NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP205990.RAinR_sr3duXPLeG5BuT6bW6JID1roheBgbT-TbY0kpR4130_provenance.