Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_assertion description "[Two deletion mutations in the hydroxymethylbilane synthase gene in two unrelated Japanese patients with acute intermittent porphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_assertion evidence source_evidence_literature NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_assertion SIO_000772 10944860 NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_assertion wasDerivedFrom befree-2016 NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_assertion wasGeneratedBy ECO_0000203 NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.
- befree-2016 importedOn "2016-02-19" NP292238.RAoCSAEGurAH_ALCXjT2In1GCcCdf6ch6YHLlbYuhOgpk130_provenance.