Matches in Nanopublications for { ?s ?p "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1192788.RAYMqwA3DEvQdKtjoKCrvOeoeXbkVaI-n3piRQW6bUR8o130_provenance.
- assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1192786.RAka5a9z1zmhZxPcOqhSPjOqdNm--LgpJmiNdBjoB3ifY130_provenance.
- NP660336.RAji94LR7Mk6xnRjU6HqwPF3Piujewy_oxuwGFI5TgfI8130_assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660336.RAji94LR7Mk6xnRjU6HqwPF3Piujewy_oxuwGFI5TgfI8130_provenance.
- NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_assertion description "[Germline mutations in SHP2 are known to cause both Noonan syndrome (NS) and LEOPARD syndrome (LS), two clinically similar autosomal dominant developmental disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660507.RAhMUI0Gix6XwMKi0zLQGtvkrcx50puKJu1_sWvMnZnWY130_provenance.