Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_assertion description "[Novel ATP1A2 mutations were found in two of the 20 families (10%)/p.Gly900Arg mutation was present in a family with epilepsy and FHM, and the p.Cys702Tyr mutation occurred in a family with occipitotemporal epilepsy and migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_assertion evidence source_evidence_literature NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_assertion SIO_000772 18028407 NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_assertion wasDerivedFrom lhgdn-20090331 NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_assertion wasGeneratedBy ECO_0000203 NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP205342.RA1KeNSs7gPd-JGS0_9T1bwhNsmWiCbL1cNpl6Audgzm4130_provenance.