Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_assertion> ?p ?o ?g. }
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- NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_assertion type Assertion NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_head.
- NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_assertion description "[Results confirm the significant contribution of ARX mutations in the etiology of X-linked mental retardation (XLMR), and imply that screening for c.428-451 dup (24 bp) mutation should be recommended in all patients with suspected XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.
- NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_assertion evidence source_evidence_literature NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.
- NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_assertion SIO_000772 16523516 NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.
- NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_assertion wasDerivedFrom lhgdn-20090331 NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.
- NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_assertion wasGeneratedBy ECO_0000203 NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.