Matches in Nanopublications for { ?s ?p "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3657.RARJCGg57ESwFl1_KqHYO47BSitK-7qgWcsanNbCsxDFs130_assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3657.RARJCGg57ESwFl1_KqHYO47BSitK-7qgWcsanNbCsxDFs130_provenance.
- NP3568.RAtzRh9b-bjedqEgv01hKXvmwMwvB2sI-H8F92GWfk828130_assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3568.RAtzRh9b-bjedqEgv01hKXvmwMwvB2sI-H8F92GWfk828130_provenance.
- NP3589.RApU44sU1GR4h9vD_ksWYxJHhYJ9HXpbIRMmOVSdQ6hjg130_assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3589.RApU44sU1GR4h9vD_ksWYxJHhYJ9HXpbIRMmOVSdQ6hjg130_provenance.
- NP3584.RA9ytTEwLdtwKNUjESnV5yTAdUjXESCeSe9ZbBLkX3Bl4130_assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3584.RA9ytTEwLdtwKNUjESnV5yTAdUjXESCeSe9ZbBLkX3Bl4130_provenance.
- NP3641.RAzkz5LaABhHZx9av3w8pde208v2qiXU6oMJXvtOY0OuI130_assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3641.RAzkz5LaABhHZx9av3w8pde208v2qiXU6oMJXvtOY0OuI130_provenance.
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- assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
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