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- source_evidence_literature type ECO_0000212 NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.
- NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_assertion description "[A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.
- NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_assertion evidence source_evidence_literature NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.
- NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_assertion SIO_000772 17668384 NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.
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- NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_assertion wasGeneratedBy ECO_0000203 NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978162.RAPWa-wlv1v5ghMDk0Q_E6E2wOo9_4TQIBrolb7qRAMWY130_provenance.