Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_assertion> ?p ?o ?g. }
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- NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_assertion type Assertion NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_head.
- NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_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." NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_provenance.
- NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_assertion evidence source_evidence_curated NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_provenance.
- NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_assertion SIO_000772 21264219 NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_provenance.
- NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_assertion wasDerivedFrom ctd_human-20130708 NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_provenance.
- NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_assertion wasGeneratedBy ECO_0000218 NP13231.RAt4DU9o3C9FwsUODtzy-do0uEg-LWktQNzrk2EzKG3AA130_provenance.