Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_assertion> ?p ?o ?g. }
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- NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_assertion type Assertion NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_head.
- NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_assertion wasGeneratedBy ECO_0000203 NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_provenance.
- NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_assertion wasDerivedFrom befree-2016 NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_provenance.
- NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_assertion SIO_000772 17056636 NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_provenance.
- NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_assertion evidence source_evidence_literature NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_provenance.
- NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_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." NP575614.RAr8PaJVpVPjZQHQRMIRq50o3eDMogUq9xjKChp6EAFRs130_provenance.