Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_assertion type Assertion NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_head.
- NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_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." NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_provenance.
- NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_assertion evidence source_evidence_literature NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_provenance.
- NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_assertion SIO_000772 22252899 NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_provenance.
- NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_assertion wasDerivedFrom befree-20140225 NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_provenance.
- NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_assertion wasGeneratedBy ECO_0000203 NP712929.RASva6VnuUHTC4lOazAIt3z_jssyG71URwLYTXZr_JLrw130_provenance.