Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_assertion> ?p ?o ?g. }
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- NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_assertion type Assertion NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_head.
- NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_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." NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.
- NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_assertion evidence source_evidence_literature NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.
- NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_assertion SIO_000772 19934113 NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.
- NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_assertion wasDerivedFrom befree-2016 NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.
- NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_assertion wasGeneratedBy ECO_0000203 NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.