Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion type Assertion NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_head.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_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." NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion evidence source_evidence_literature NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion SIO_000772 20538404 NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion wasDerivedFrom befree-2016 NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion wasGeneratedBy ECO_0000203 NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.