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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. }

• 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.
• 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.
• 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.
• NP230065.RA9YRWZyWVPYZHcCoifoGNERyiCB0YwPgwLhrhfHxK5eY130_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." NP230065.RA9YRWZyWVPYZHcCoifoGNERyiCB0YwPgwLhrhfHxK5eY130_provenance.
• NP4576.RA-QCQn2rGYmurtWgGFS1Lg0dkTzXyq1EjR4SwSOtSzzY130_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." NP4576.RA-QCQn2rGYmurtWgGFS1Lg0dkTzXyq1EjR4SwSOtSzzY130_provenance.
• NP555717.RAyHZ8wcB8s2xMEPfY_BBqEbzoSMvoFxJeui_8OwSiOb0130_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." NP555717.RAyHZ8wcB8s2xMEPfY_BBqEbzoSMvoFxJeui_8OwSiOb0130_provenance.
• NP4575.RAR5tmPaBtSEaBLhYG8k38dRWu0YaPekIy5fOCe78Avvc130_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." NP4575.RAR5tmPaBtSEaBLhYG8k38dRWu0YaPekIy5fOCe78Avvc130_provenance.
• NP4577.RAWWQLchRJDGFGt8M_rlbaOsVm51xXGyyMwPS2E05WsnA130_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." NP4577.RAWWQLchRJDGFGt8M_rlbaOsVm51xXGyyMwPS2E05WsnA130_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.
• 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.
• NP4578.RAH-T8Bf_WbGA5zNjb5fFrnfFFd2R19GQhzTSuraUqNx0130_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." NP4578.RAH-T8Bf_WbGA5zNjb5fFrnfFFd2R19GQhzTSuraUqNx0130_provenance.
• NP4579.RAL1LskTX_1cLsR5Ktdr6iR95T1O6DUTX7N5TlamX-XFo130_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." NP4579.RAL1LskTX_1cLsR5Ktdr6iR95T1O6DUTX7N5TlamX-XFo130_provenance.
• NP555716.RAmU1wARYiK53axV0f8u2dAFDSvPTRtjNalOUCEFUraxI130_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." NP555716.RAmU1wARYiK53axV0f8u2dAFDSvPTRtjNalOUCEFUraxI130_provenance.