Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion> ?p ?o ?g. }
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- NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion type Assertion NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_head.
- NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion description "[Human acute intermittent porphyria (AIP), the most common acute hepatic porphyria, is an autosomal dominant inborn error of heme biosynthesis due to the half-normal activity of hydroxymethylbilane synthase (HMB-synthase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_provenance.
- NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion evidence source_evidence_literature NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_provenance.
- NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion SIO_000772 19934113 NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_provenance.
- NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion wasDerivedFrom befree-20140225 NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_provenance.
- NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_assertion wasGeneratedBy ECO_0000203 NP921376.RADsQYBwa8BS6ZGL450pIFC0pdgkAprh6-V3uNsPbTkdY130_provenance.