Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_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." NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_assertion evidence source_evidence_literature NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_assertion SIO_000772 19934113 NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_assertion wasDerivedFrom befree-20150227 NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_assertion wasGeneratedBy ECO_0000203 NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP459231.RAak_5_KuJcA6Guv7cauVUhXe-418Kszdn02YuKQwKFoY130_provenance.