Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP144155.RAALPnlIJHTGIlhqd57D1SRiAPwsI7SGyQ8Xwz7_GpN0k130_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." NP144155.RAALPnlIJHTGIlhqd57D1SRiAPwsI7SGyQ8Xwz7_GpN0k130_provenance.
- NP123468.RArn9RrdfETykUuZQVRc77i-BndLWGuFub86oDmY_-Cxk130_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." NP123468.RArn9RrdfETykUuZQVRc77i-BndLWGuFub86oDmY_-Cxk130_provenance.
- 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." provenance.
- 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." provenance.
- NP226759.RAlZ4gt2qRGCvRF-xCeJ41Q4SsoLr8hoNlIauIU0uoJeU130_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." NP226759.RAlZ4gt2qRGCvRF-xCeJ41Q4SsoLr8hoNlIauIU0uoJeU130_provenance.
- NP207296.RAxdeXpdHiVduIlOYatLajc82iN4n35L_U3rk3wm1fomI130_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." NP207296.RAxdeXpdHiVduIlOYatLajc82iN4n35L_U3rk3wm1fomI130_provenance.
- 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.
- NP226760.RAMQzRKUfRW93Y-JbLQBBxJnRhvVvJ3ucawrUyWAFt7xs130_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." NP226760.RAMQzRKUfRW93Y-JbLQBBxJnRhvVvJ3ucawrUyWAFt7xs130_provenance.