Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_assertion type Assertion NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_head.
- NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_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." NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_provenance.
- NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_assertion evidence source_evidence_literature NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_provenance.
- NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_assertion SIO_000772 12874405 NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_provenance.
- NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_assertion wasDerivedFrom befree-20140225 NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_provenance.
- NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_assertion wasGeneratedBy ECO_0000203 NP884280.RA45lX4PGRNPXFp0yVGjAWYKu_ZsiO8XsCQfOpIVsw1mA130_provenance.