Matches in Nanopublications for { ?s ?p "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975751.RAA5o7ZuUBSKWys2VRr5IFmAed6YDQI_DCSjVT5kfWVhE130_provenance.
- NP975753.RAAxclTjFZxWaES0WSKWX8L3drOd-p0MBaRONf69NU5C0130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975753.RAAxclTjFZxWaES0WSKWX8L3drOd-p0MBaRONf69NU5C0130_provenance.
- NP660335.RAH32VZUteJGq2oocGZjX8IshERCceeFG6Yy4Uu-KtV6I130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660335.RAH32VZUteJGq2oocGZjX8IshERCceeFG6Yy4Uu-KtV6I130_provenance.
- NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660499.RAIA67HAZufBUssXjvtkeFaR2uos7B3OKCMalUlVdb0cs130_provenance.
- NP660548.RAFFzjrrduFTH0S8BdiXdPA7id7lOEXE0hdhO3o_wTCtw130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660548.RAFFzjrrduFTH0S8BdiXdPA7id7lOEXE0hdhO3o_wTCtw130_provenance.
- assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975754.RAME9woOlwomynADdifsOBKEbVE9G03RinTn8FWJ0GAak130_provenance.
- NP660556.RAqo_99lFsvIqQ7y4gHUwIhGYMUxtn5PqhkCBdX5G65DU130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660556.RAqo_99lFsvIqQ7y4gHUwIhGYMUxtn5PqhkCBdX5G65DU130_provenance.
- NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_assertion description "[Finally, mutations in the Ptpn11 gene (encoding SHP-2) underlie the developmental disorders Noonan syndrome and Leopard syndrome characterized by congenital heart disease and hematologic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP975752.RAr5-fUeEQA22OfjyxeLKc19cjBNEva3BQjRP8v9R62iI130_provenance.