Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP777409.RA4N-hmBDVpQ7nhJ9J2rEjc4eMcghJggy5naxh4sEydCg130_provenance.