Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_assertion> ?p ?o ?g. }
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- NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_assertion type Assertion NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_head.
- NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_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." NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_provenance.
- NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_assertion evidence source_evidence_literature NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_provenance.
- NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_assertion SIO_000772 21264219 NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_provenance.
- NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_assertion wasDerivedFrom befree-20150227 NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_provenance.
- NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_assertion wasGeneratedBy ECO_0000203 NP253411.RAajAsj8VcUWNxmseS8xWpVnSwu0ctDm3zKwDxw4cJ_UE130_provenance.