Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_assertion type Assertion NP126798.RAswKorahqmbZs9oVyGoW-82E3rSv421R4LquAveredLE130_head.
- 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.