Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion> ?p ?o ?g. }
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- NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion type Assertion NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_head.
- NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion wasGeneratedBy ECO_0000203 NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_provenance.
- NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion wasDerivedFrom befree-20150227 NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_provenance.
- NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion SIO_000772 24935154 NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_provenance.
- NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion evidence source_evidence_literature NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_provenance.
- NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_provenance.