Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion> ?p ?o ?g. }
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- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion type Assertion NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_head.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_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." NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion evidence source_evidence_literature NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion SIO_000772 20538404 NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion wasDerivedFrom befree-20140225 NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.
- NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_assertion wasGeneratedBy ECO_0000203 NP563189.RAtk-lfZhy87doMJneUyxzb4t42J8Fx4heMOLqFQGg_rw130_provenance.