Matches in Nanopublications for { ?s ?p "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP386198.RAh4-v0x_CEmDH7hKsIuzSMvqPY1YB-rwBmhMCAszH6v8130_assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386198.RAh4-v0x_CEmDH7hKsIuzSMvqPY1YB-rwBmhMCAszH6v8130_provenance.
- NP699377.RALSRrW-BpSvorTOkSXSi1GTzslpWTc9NL7U9Sbbh0afc130_assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699377.RALSRrW-BpSvorTOkSXSi1GTzslpWTc9NL7U9Sbbh0afc130_provenance.
- assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.