Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_assertion description "[Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_assertion evidence source_evidence_curated NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_assertion SIO_000772 2384601 NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_assertion wasDerivedFrom uniprot-20130724 NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_assertion wasGeneratedBy ECO_0000218 NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6348.RADZff6bIwnvufY-dOLHU5T77fgOitRzfNfmA7V5sWJLM130_provenance.