Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_assertion type Assertion NP402766.RAB9QgA79OK5izIXeK160BRj9FM7H7TpfcJe3hbC-On5A130_head.
- 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.