Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_assertion type Assertion NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_head.
- NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_assertion description "[Mutations in the Aristaless-related homeobox gene (ARX) are associated with a wide variety of neurologic disorders including lissencephaly, hydrocephaly, West syndrome, Partington syndrome, and X-linked intellectual disability with or without epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_provenance.
- NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_assertion evidence source_evidence_literature NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_provenance.
- NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_assertion SIO_000772 22252899 NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_provenance.
- NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_assertion wasDerivedFrom befree-20140225 NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_provenance.
- NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_assertion wasGeneratedBy ECO_0000203 NP639069.RA_r73JwdFkHmzREYbaL9YD1hky4ntoVL3MHdN20ilVsI130_provenance.