Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_assertion> ?p ?o ?g. }
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- NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_assertion type Assertion NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_head.
- NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_assertion description "[The common ACE deletion polymorphism is associated with a greater than 2-fold increase in the odds of developing JET in children undergoing surgical repair of atrioventricular septal defect, Tetralogy of Fallot, ventricular septal defect or the Norwood and arterial switch procedures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_provenance.
- NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_assertion evidence source_evidence_literature NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_provenance.
- NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_assertion SIO_000772 21740877 NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_provenance.
- NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_assertion wasDerivedFrom befree-2016 NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_provenance.
- NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_assertion wasGeneratedBy ECO_0000203 NP908245.RADyakP6SWGJvUf1dR2gNgb6Mpxy3yKjvuiHYe_erhFsQ130_provenance.