Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_assertion description "[Molecular defect of a phosphoglycerate kinase variant (PGK-Matsue) associated with hemolytic anemia: Leu----Pro substitution caused by T/A----C/G transition in exon 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_assertion evidence source_evidence_curated NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_assertion SIO_000772 2001457 NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_assertion wasDerivedFrom uniprot-20150221 NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_assertion wasGeneratedBy ECO_0000218 NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP691.RAoI7LPXh4vlWmWgc7NaYRkH1C_Lsr8GziZ6sCR1cdYwo130_provenance.