Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_assertion description "[Mutations in SMC3 cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_assertion evidence source_evidence_literature NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_assertion SIO_000772 17273969 NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_assertion wasDerivedFrom lhgdn-20090331 NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_assertion wasGeneratedBy ECO_0000203 NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP222519.RA1MG6EhyE9nY4ByGkbnAERHfgEucPaxctHk30hz2a-CQ130_provenance.