Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_assertion wasGeneratedBy ECO_0000218 NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_assertion wasDerivedFrom ctd_human-2016 NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_assertion SIO_000772 8064810 NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_assertion evidence source_evidence_curated NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.
- NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_assertion description "[A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP36868.RA5UJ9GV-Ru6JFoz9YOCOzchnq-MSL5LYtD76tfsIHP34130_provenance.