Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_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." NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_assertion evidence source_evidence_literature NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_assertion SIO_000772 12874405 NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_assertion wasDerivedFrom befree-20140225 NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_assertion wasGeneratedBy ECO_0000203 NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP590640.RAdQUfgPAN60LU-VhiTjpAxrikH3xfLd8QlggpTZBDCW8130_provenance.