Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_assertion evidence source_evidence_curated NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_assertion SIO_000772 9329347 NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_assertion wasDerivedFrom ctd_human-2016 NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_assertion wasGeneratedBy ECO_0000218 NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP37620.RAL2LumQepaTmIKrY11lHvQbbgG9ttXKlKQx9cl3SHjaQ130_provenance.