Matches in Nanopublications for { ?s ?p "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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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- NP159791.RArlpU7cKqxE0cKKETeo_y08abk8wsIwP-1cLwS6n_1W0130_assertion description "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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." NP159791.RArlpU7cKqxE0cKKETeo_y08abk8wsIwP-1cLwS6n_1W0130_provenance.
- NP507162.RARWDZuN9kgYW8md6Bp8N62P1x9pOGa3Pd4eZ6QAqq0gE130_assertion description "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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." NP507162.RARWDZuN9kgYW8md6Bp8N62P1x9pOGa3Pd4eZ6QAqq0gE130_provenance.
- NP28111.RA5zbzW4uV55ravUqLSSxDnb4iQamSkkmpipGPKR5YmSc130_assertion description "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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." NP28111.RA5zbzW4uV55ravUqLSSxDnb4iQamSkkmpipGPKR5YmSc130_provenance.
- assertion description "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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 "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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.
- NP899559.RAOCuY8gLUtx35eDZqxCEO-VLVRpgJfzYHEn3a2otggQQ130_assertion description "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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." NP899559.RAOCuY8gLUtx35eDZqxCEO-VLVRpgJfzYHEn3a2otggQQ130_provenance.
- NP664291.RABFrtBlsVmToZCfQCgr_CTU4RRXOVXQ7UBS34CM1ztuQ130_assertion description "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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." NP664291.RABFrtBlsVmToZCfQCgr_CTU4RRXOVXQ7UBS34CM1ztuQ130_provenance.
- NP617876.RAoc0u8hmUfVcOj--tw2WkpG_kDjtys-Et7HXicX-ECtk130_assertion description "[We have identified five different mutations in RAF1 in ten individuals with Noonan syndrome; those with any of four mutations causing changes in the CR2 domain of RAF1 had hypertrophic cardiomyopathy (HCM), whereas affected individuals 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." NP617876.RAoc0u8hmUfVcOj--tw2WkpG_kDjtys-Et7HXicX-ECtk130_provenance.