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- NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_assertion type Assertion NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_head.
- NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_assertion wasGeneratedBy ECO_0000203 NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_provenance.
- NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_assertion wasDerivedFrom befree-2016 NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_provenance.
- NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_assertion SIO_000772 17056636 NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_provenance.
- NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_assertion evidence source_evidence_literature NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_provenance.
- NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_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." NP575615.RASt99xFCQcJLetW547eZ5NzB4zIj7XPN-aE00npDfMk0130_provenance.