Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion> ?p ?o ?g. }
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- NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion type Assertion NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_head.
- NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion description "[Mutations in cohesin complex members SMC3 and SMC1A 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." NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion evidence source_evidence_literature NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion SIO_000772 17273969 NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion wasDerivedFrom befree-20150227 NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_assertion wasGeneratedBy ECO_0000203 NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.