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- NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_assertion type Assertion NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_head.
- NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_assertion wasGeneratedBy ECO_0000203 NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_provenance.
- NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_assertion wasDerivedFrom befree-20150227 NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_provenance.
- NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_assertion SIO_000772 17056636 NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_provenance.
- NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_assertion evidence source_evidence_literature NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_provenance.
- NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_assertion description "[We further defined the phenotypic spectrum associated with KRAS missense mutations and provided the first evidence of clinical differences in patients with KRAS mutations compared with Noonan syndrome affected individuals with heterozygous PTPN11 mutations and CFC patients carrying a BRAF, MEK1 or MEK1 alteration, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660709.RAg3oEKiUB4-ZZMKLS_hafzDwN23EqJ0jDfWPgifD-PpA130_provenance.