Matches in Nanopublications for { ?s ?p "[We have recently demonstrated that two inherited skin diseases, Vohwinkel's syndrome (VS) and progressive symmetric erythrokeratoderma (PSEK) may result from mutations in the gene encoding loricrin, a major constituent of the CE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_assertion description "[We have recently demonstrated that two inherited skin diseases, Vohwinkel's syndrome (VS) and progressive symmetric erythrokeratoderma (PSEK) may result from mutations in the gene encoding loricrin, a major constituent of the CE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658377.RAAr4yNMViLUR2YPOsFWKl6otFXJT9oVAo93i5AxwXE-c130_provenance.
- NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_assertion description "[We have recently demonstrated that two inherited skin diseases, Vohwinkel's syndrome (VS) and progressive symmetric erythrokeratoderma (PSEK) may result from mutations in the gene encoding loricrin, a major constituent of the CE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP751833.RA6qoTh6Qj_6eTY1ZpUWby6L9YU_dweKyN-luea7ezNBU130_provenance.