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- source_evidence_literature type ECO_0000212 NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_assertion description "[Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_assertion evidence source_evidence_literature NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_assertion SIO_000772 19738637 NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_assertion wasDerivedFrom befree-20150227 NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_assertion wasGeneratedBy ECO_0000203 NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978163.RAqEnpkih5LmlLo5z1VenrtzTTd5UbV6H-ra9JxXXchrQ130_provenance.