Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP215983.RA0DvQoTPhWiuyxuDJwGiPCF82hPWqJ2oqMIAZLKmV-X0130_provenance.