Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion> ?p ?o ?g. }
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- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion type Assertion NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_head.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion wasGeneratedBy ECO_0000203 NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion wasDerivedFrom befree-20140225 NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion SIO_000772 17056636 NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion evidence source_evidence_literature NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.
- NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_assertion description "[Remarkably, our cohort of individuals with KRAS mutations showed a high clinical variability, ranging from Noonan syndrome to CFC, and also included two patients who met the clinical criteria of Costello syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP624928.RAJyW6EYdgGaVKUBH8m-ZG-3ZgcFF3siOczr1WC19D2qg130_provenance.