Matches in Nanopublications for { ?s ?p "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 9 of
9
with 100 items per page.
- assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP710274.RA7NJVy0JTD3yOCKSlG0Vm40xm4QF_uOnJT7cZZhB4lQI130_assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710274.RA7NJVy0JTD3yOCKSlG0Vm40xm4QF_uOnJT7cZZhB4lQI130_provenance.
- NP611787.RAuJbe6tqJiZ20-7WsqVr_BvlJhPbdmkt47ZIg1ojwBzQ130_assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611787.RAuJbe6tqJiZ20-7WsqVr_BvlJhPbdmkt47ZIg1ojwBzQ130_provenance.
- NP401723.RAMypJVsQxU-9eRg3qN-GPcZrHGfqPWDzHB72CQKAi_Nk130_assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401723.RAMypJVsQxU-9eRg3qN-GPcZrHGfqPWDzHB72CQKAi_Nk130_provenance.
- NP611785.RAEkF7C3ncv5vpMOuR7Mmty_C5_HXTq4fVfaIIjq7is1U130_assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611785.RAEkF7C3ncv5vpMOuR7Mmty_C5_HXTq4fVfaIIjq7is1U130_provenance.
- NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_assertion description "[Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611788.RALi9PXj7hvBcep_baQwIgMBfH0qsfxqshus7vmwjZs0s130_provenance.