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- source_evidence_literature type ECO_0000212 NP978168.RAXG0_3EcwcIXJ8tS_ZLR4wwQgFb8KrKgzziyLu4CEH-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978168.RAXG0_3EcwcIXJ8tS_ZLR4wwQgFb8KrKgzziyLu4CEH-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978168.RAXG0_3EcwcIXJ8tS_ZLR4wwQgFb8KrKgzziyLu4CEH-U130_provenance.
- NP978168.RAXG0_3EcwcIXJ8tS_ZLR4wwQgFb8KrKgzziyLu4CEH-U130_assertion description "[Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978168.RAXG0_3EcwcIXJ8tS_ZLR4wwQgFb8KrKgzziyLu4CEH-U130_provenance.
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