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- source_evidence_literature type ECO_0000212 NP978115.RAPDa_CNw-pyKcbo4PpPwrVsZ_yP4BHxr44JFteAR-3l0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978115.RAPDa_CNw-pyKcbo4PpPwrVsZ_yP4BHxr44JFteAR-3l0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978115.RAPDa_CNw-pyKcbo4PpPwrVsZ_yP4BHxr44JFteAR-3l0130_provenance.
- NP978115.RAPDa_CNw-pyKcbo4PpPwrVsZ_yP4BHxr44JFteAR-3l0130_assertion description "[Mutations in the human aristaless-related homeobox (ARX) gene are amongst the major causes of developmental and neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978115.RAPDa_CNw-pyKcbo4PpPwrVsZ_yP4BHxr44JFteAR-3l0130_provenance.
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- NP978115.RAPDa_CNw-pyKcbo4PpPwrVsZ_yP4BHxr44JFteAR-3l0130_assertion SIO_000772 22642246 NP978115.RAPDa_CNw-pyKcbo4PpPwrVsZ_yP4BHxr44JFteAR-3l0130_provenance.
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