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- source_evidence_literature type ECO_0000212 NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_assertion description "[The authors assessed ARX as a candidate gene for XLAG in a genetic analysis of neuronal migration disorders and found two different point mutations in two XLAG pedigrees affecting the homeodomain of the protein, confirming that ARX is a causative gene for XLAG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_assertion evidence source_evidence_literature NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_assertion SIO_000772 12874405 NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_assertion wasDerivedFrom befree-2016 NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_assertion wasGeneratedBy ECO_0000203 NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.
- befree-2016 importedOn "2016-02-19" NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_provenance.