Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_assertion type Assertion NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_head.
- NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_assertion description "[Aristaless-related homeobox gene (ARX) mutation leads to several neurological disorders including X-linked lissencephaly with abnormal genitalia (XLAG), West syndrome and Partington syndrome, with XLAG being the most severe form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_provenance.
- NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_assertion evidence source_evidence_literature NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_provenance.
- NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_assertion SIO_000772 20538404 NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_provenance.
- NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_assertion wasDerivedFrom befree-2016 NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_provenance.
- NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_assertion wasGeneratedBy ECO_0000203 NP817892.RA38ojvObSos4qLHHRZuNEDJqHqAcKWT6Pk0zDhyj1kxc130_provenance.