Matches in Nanopublications for { ?s ?p "[Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP5487.RAnB2EhAbDdfNJGhB1U0cPq072TCTfZFlWeLQJTHhCVtw130_assertion description "[Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5487.RAnB2EhAbDdfNJGhB1U0cPq072TCTfZFlWeLQJTHhCVtw130_provenance.
- assertion description "[Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP384.RAgFBTM8nONxVzv0WmpJw-QfA7ci1ZvNcE3-ZkCtubp-A130_assertion description "[Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP384.RAgFBTM8nONxVzv0WmpJw-QfA7ci1ZvNcE3-ZkCtubp-A130_provenance.