Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_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." NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_assertion evidence source_evidence_curated NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_assertion SIO_000772 8064810 NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_assertion wasDerivedFrom ctd_human-20130708 NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_assertion wasGeneratedBy ECO_0000218 NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP8316.RAwPWlD78z49r-gdrvcMkajIj0E9KGIbTa93k0kt9ei50130_provenance.