Matches in Nanopublications for { ?s ?p "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427469.RAhXq_Lp-JrV_cIowC7q7Q-dJ44k-HOChiNx1lFvI05mI130_provenance.
- NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP161839.RAzCnlBMn8G7cYgCvN_Wkd93yC4SVCmxwun2U9I1rMWcc130_provenance.
- assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319173.RA22KmiUvLnNPqi0jELN0myeyQ6XH2tFgHrlkJPyDjvuQ130_provenance.