Matches in Nanopublications for { ?s ?p "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP911927.RA1W8BNUhNgVUwh8qiAkJHaPi4AEA9l3luOVqwiYIR1Xk130_assertion description "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911927.RA1W8BNUhNgVUwh8qiAkJHaPi4AEA9l3luOVqwiYIR1Xk130_provenance.
- NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_assertion description "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611966.RAOITJRMaHNjSKqegP5OE7cY19FiN8jS4nFPWzemJGnzw130_provenance.
- assertion description "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP797403.RAjF5OUJ05YxWQmMb66ibih1XqZa-lJktZJNjXng66J8o130_assertion description "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797403.RAjF5OUJ05YxWQmMb66ibih1XqZa-lJktZJNjXng66J8o130_provenance.