Matches in Nanopublications for { ?s ?p "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989707.RATgdEZDQ9_Q90DmjUyouMEe4gE9-7VrlrnArWhhsJM0Y130_provenance.
- NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989770.RAQHr6ON-PW-853Z495x57tmfhBvQuNO4UT8WN5goWWK4130_provenance.
- NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155958.RAeRWP74A3kcFzLBavVfWqUdmhiJwV6iGCmy-wmdBLO1Q130_provenance.
- NP1155963.RAYhFkoymx_kHJSwOihP52T2qsmJeuUcra_FMboJ43FmE130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155963.RAYhFkoymx_kHJSwOihP52T2qsmJeuUcra_FMboJ43FmE130_provenance.
- assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_provenance.
- NP1155956.RAjUbpzWIc7Qly53nCJ2NdipQoowWQwI6Xk2Itrdx44aU130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155956.RAjUbpzWIc7Qly53nCJ2NdipQoowWQwI6Xk2Itrdx44aU130_provenance.