Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_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." NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_assertion evidence source_evidence_literature NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_assertion SIO_000772 17273969 NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_assertion wasDerivedFrom lhgdn-20090331 NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_assertion wasGeneratedBy ECO_0000203 NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_provenance.