Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_assertion wasGeneratedBy ECO_0000203 NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_assertion wasDerivedFrom lhgdn-20090331 NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_assertion SIO_000772 12838518 NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_assertion evidence source_evidence_literature NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.
- NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_assertion description "[Missense DCX mutations may manifest as non-syndromic mental retardation with cryptogenic epilepsy in female subjects and subcortical band heterotopia (SBH) in boys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200382.RAAp17epla0oosLBQo8Lgc5sYxyA4ZDhcVFE519uTaS2k130_provenance.