Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_assertion type Assertion NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_head.
- NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_assertion description "[Mutations in the aristaless-related homeobox (ARX) gene are associated with multiple neurologic disorders in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_provenance.
- NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_assertion evidence source_evidence_literature NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_provenance.
- NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_assertion SIO_000772 18799476 NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_provenance.
- NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_assertion wasDerivedFrom befree-20150227 NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_provenance.
- NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_assertion wasGeneratedBy ECO_0000203 NP978112.RAtIFf6VYuaIgaBn5O4OkSlBiTHIXPmU_HRy2nZcM3wAA130_provenance.