Matches in Nanopublications for { ?s ?p "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- NP616480.RAVIc985H4xbwB0MiexyVvl79yzQUOVBmyinVaIFwDda0130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616480.RAVIc985H4xbwB0MiexyVvl79yzQUOVBmyinVaIFwDda0130_provenance.
- assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767240.RAqmHDkSmSW2x9E4Mu4V5ogd-6-qGBBym6TeBl2dLY1CY130_provenance.
- NP767277.RAtp5-5fH40yz5cHOyNqqZVETZZCGXqhSGndEdc2HGsBI130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767277.RAtp5-5fH40yz5cHOyNqqZVETZZCGXqhSGndEdc2HGsBI130_provenance.
- NP256924.RABi0EGBJtz-cpVEk_ukleRx7QhDmWUlI8t-m-uycQtg0130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256924.RABi0EGBJtz-cpVEk_ukleRx7QhDmWUlI8t-m-uycQtg0130_provenance.
- NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_provenance.
- NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.