Matches in Nanopublications for { ?s ?p "[Uroporphyrinogen decarboxylase (URO-D) deficiency is responsible for two forms of genetic cutaneous porphyria: familial porphyria cutanea tarda (f-PCT) and hepatoerythropoietic porphyria (HEP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Uroporphyrinogen decarboxylase (URO-D) deficiency is responsible for two forms of genetic cutaneous porphyria: familial porphyria cutanea tarda (f-PCT) and hepatoerythropoietic porphyria (HEP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP767200.RAgQkm1jQsNDkzVLHYy_3dq45TrKL_8el8OsZvYrnJTe8130_assertion description "[Uroporphyrinogen decarboxylase (URO-D) deficiency is responsible for two forms of genetic cutaneous porphyria: familial porphyria cutanea tarda (f-PCT) and hepatoerythropoietic porphyria (HEP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767200.RAgQkm1jQsNDkzVLHYy_3dq45TrKL_8el8OsZvYrnJTe8130_provenance.
- NP294568.RA5UP73N_dyfbZf_APJFp8hOEYGfYFkHgr9L3IQqtDa6U130_assertion description "[Uroporphyrinogen decarboxylase (URO-D) deficiency is responsible for two forms of genetic cutaneous porphyria: familial porphyria cutanea tarda (f-PCT) and hepatoerythropoietic porphyria (HEP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294568.RA5UP73N_dyfbZf_APJFp8hOEYGfYFkHgr9L3IQqtDa6U130_provenance.