Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_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." NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_assertion evidence source_evidence_curated NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_assertion SIO_000772 9329347 NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_assertion wasDerivedFrom uniprot-20130724 NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_assertion wasGeneratedBy ECO_0000218 NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP302.RArXDe90Zb2V_XrwqvLQRYF6n60_orTD1ZH4U9kb2XTBc130_provenance.