Matches in Nanopublications for { ?s ?p "[Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3663.RAeo2keGPY6AkkLKDqB9I8IMwt5-2ahrFVk5J7iGFtnUc130_assertion description "[Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3663.RAeo2keGPY6AkkLKDqB9I8IMwt5-2ahrFVk5J7iGFtnUc130_provenance.
- assertion description "[Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1992.RAmtsdRdgWI3QntYltZmMce77boAultS6tc6ePD_dIN0E130_assertion description "[Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1992.RAmtsdRdgWI3QntYltZmMce77boAultS6tc6ePD_dIN0E130_provenance.