Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP793317.RAaCh8IgO8HRl5LBZF4ni7EOUL6xTXlW-oTQ6FrAAD_LI130_provenance.