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- source_evidence_literature type ECO_0000212 NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_assertion description "[ARX mutation testing should be undertaken in children aged less than 1 year with Ohtahara syndrome and a movement disorder, and in infants with unexplained neurodegeneration, progressive white matter loss, and cortical atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_assertion evidence source_evidence_literature NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_assertion SIO_000772 19747203 NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_assertion wasDerivedFrom befree-20150227 NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_assertion wasGeneratedBy ECO_0000203 NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978109.RAg7ttRPpbgl6D9isM0FEiUc_-R0E-ffxabNCrl7uzquA130_provenance.