Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276604.RAD7Vh97pXxiTqKI9Oj3pRJwMffEzPiHVeJsq-ybFrKW8130_provenance.
• NP665846.RAcL2oiSRBzTzNAow0Bd-5dMflEkY6sQuyVLxEMtef4ZM130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665846.RAcL2oiSRBzTzNAow0Bd-5dMflEkY6sQuyVLxEMtef4ZM130_provenance.
• NP660331.RADYBxC271jwGGTCcxTUM7xJJFTwrjmBSkqcRKKJ1-W90130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660331.RADYBxC271jwGGTCcxTUM7xJJFTwrjmBSkqcRKKJ1-W90130_provenance.
• NP641442.RALuNOyodaCfEp1N_c4OOrKEapiLKvEEC3mphhMrDUbHs130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641442.RALuNOyodaCfEp1N_c4OOrKEapiLKvEEC3mphhMrDUbHs130_provenance.
• NP750084.RA0hF0ZU8bDZkAWlFIVch34iaqDJ3uOTotBc3Loy461KY130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750084.RA0hF0ZU8bDZkAWlFIVch34iaqDJ3uOTotBc3Loy461KY130_provenance.
• NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584872.RADXjfIF4bQQJDbzK809ANXFI1PYDzxNfV6js49tS9NJM130_provenance.
• NP221009.RAwoz3lK-naynzwM5ogBrKuW71s_Z94_V__-mLbuEAkbw130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221009.RAwoz3lK-naynzwM5ogBrKuW71s_Z94_V__-mLbuEAkbw130_provenance.
• NP584870.RA3Sqwp0MloAWeVMFYHLM0-5cXPHlKRuiXFZXhmnap7hc130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584870.RA3Sqwp0MloAWeVMFYHLM0-5cXPHlKRuiXFZXhmnap7hc130_provenance.
• NP584871.RA4Kxq6LLc6h5pEODeWvhmWqtamXg-ZOq279fnGfZC8c0130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584871.RA4Kxq6LLc6h5pEODeWvhmWqtamXg-ZOq279fnGfZC8c0130_provenance.
• NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660660.RAHJsUUXG7RU68ZjiKpyFw4c4hRgAeY46b2ETsa6yFZA0130_provenance.
• NP220869.RAhkX-PGaVbiWTvc5kxvdj4DLoG_6glW279BnUxLPwJC8130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220869.RAhkX-PGaVbiWTvc5kxvdj4DLoG_6glW279BnUxLPwJC8130_provenance.
• NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221102.RAij1XWwr9Gu5QqqoYlTS3D_pkmAqoJhJNCl6Nvrw0Jrc130_provenance.
• NP584868.RAF37EddgdrplZC4aMQK7wCBjyPqqsIOqipRQmY-SF044130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584868.RAF37EddgdrplZC4aMQK7wCBjyPqqsIOqipRQmY-SF044130_provenance.
• NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_assertion description "[Mutations of the protein tyrosine phosphatase SHP-2 are implicated in human diseases, causing Noonan syndrome (NS) and related developmental disorders or contributing to leukemogenesis depending on the specific amino acid substitution involved.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584869.RAMYbQ4L-8JE--eqavdGSbhus3eMU9P034ts3yC981S8Y130_provenance.