Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_assertion description "[Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_assertion evidence source_evidence_curated NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_assertion SIO_000772 3383242 NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_assertion wasDerivedFrom ctd_human-20130708 NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_assertion wasGeneratedBy ECO_0000218 NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP8439.RA_efF_kbdnJfTgCp1x5rXQi0U_sX2FlStFa8Pi3LxgsM130_provenance.