Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_assertion> ?p ?o ?g. }
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- NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_assertion type Assertion NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_head.
- NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_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." NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_provenance.
- NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_assertion evidence source_evidence_curated NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_provenance.
- NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_assertion SIO_000772 21264219 NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_provenance.
- NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_assertion wasDerivedFrom ctd_human-20130708 NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_provenance.
- NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_assertion wasGeneratedBy ECO_0000218 NP13233.RATcUaxACbFTiAuYumh_toWlC1KmxyB5Rk9_GTfg3xCPI130_provenance.