Matches in Nanopublications for { ?s ?p "[Congenital erythropoietic porphyria (CEP; Gunther disease; OMIM 263700) is a rare autosomal recessive disorder caused by a deficiency of uroporphyrinogen III synthase (UROS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Congenital erythropoietic porphyria (CEP; Gunther disease; OMIM 263700) is a rare autosomal recessive disorder caused by a deficiency of uroporphyrinogen III synthase (UROS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP480295.RAVtEbtgyw1-z6jDffL63MGHgw9oeCnrUiVbQ_Bn0aGLA130_assertion description "[Congenital erythropoietic porphyria (CEP; Gunther disease; OMIM 263700) is a rare autosomal recessive disorder caused by a deficiency of uroporphyrinogen III synthase (UROS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480295.RAVtEbtgyw1-z6jDffL63MGHgw9oeCnrUiVbQ_Bn0aGLA130_provenance.