Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_assertion> ?p ?o ?g. }
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- NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_assertion type Assertion NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_head.
- 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.
- NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_assertion evidence source_evidence_literature NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_provenance.
- NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_assertion SIO_000772 10397714 NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_provenance.
- NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_assertion wasDerivedFrom befree-20150227 NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_provenance.
- NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_assertion wasGeneratedBy ECO_0000203 NP767195.RACcDjzkdOzKtugNM-ho6Ekiqs0ZLKWR4S5h3IVVVSFVI130_provenance.