Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_assertion> ?p ?o ?g. }
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- NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_assertion type Assertion NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_head.
- NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_assertion description "[Study identified 5 mutations in RAF1 in 10 individuals with Noonan syndrome; those with mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy, while those with mutations leading to changes in the CR3 domain did not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_provenance.
- NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_assertion evidence source_evidence_literature NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_provenance.
- NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_assertion SIO_000772 17603482 NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_provenance.
- NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_assertion wasDerivedFrom lhgdn-20090331 NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_provenance.
- NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_assertion wasGeneratedBy ECO_0000203 NP186653.RAIyLCe3FjSks3xFlbalWvC6EYBztdgb0NQZYEGknY8mE130_provenance.