Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion type Assertion NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_head.
- NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_provenance.
- NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion evidence source_evidence_literature NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_provenance.
- NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion SIO_000772 21264219 NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_provenance.
- NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion wasDerivedFrom befree-20140225 NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_provenance.
- NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_assertion wasGeneratedBy ECO_0000203 NP263317.RAieOqYKCqP4PCsW4C-IOmd3m-JLwFVf5hmGKV9FIgcH0130_provenance.