Matches in Nanopublications for { ?s ?p "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP899660.RA3sz7GrbNzjgm5DPvRoT2NBd0_dqpNWyWkxkhjyo3nVY130_assertion description "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899660.RA3sz7GrbNzjgm5DPvRoT2NBd0_dqpNWyWkxkhjyo3nVY130_provenance.
- NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_assertion description "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_provenance.
- NP401293.RApVbOJwvfjhEoTlVt9L7zMSCTOGP7fbHiSD3jIwNvy9s130_assertion description "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401293.RApVbOJwvfjhEoTlVt9L7zMSCTOGP7fbHiSD3jIwNvy9s130_provenance.
- NP630574.RAPWXoa8TGeguK_ZNjOeHKIAUC7WXMFMYBSIlFGsM14_0130_assertion description "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630574.RAPWXoa8TGeguK_ZNjOeHKIAUC7WXMFMYBSIlFGsM14_0130_provenance.
- NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_assertion description "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_provenance.