Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_assertion description "[Mutations in the ABCC8 (SUR1 subunit of the K(ATP) channel) gene are associated with a variable clinical phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_assertion evidence source_evidence_literature NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_assertion SIO_000772 19021632 NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_assertion wasDerivedFrom gad-20150221 NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_assertion wasGeneratedBy ECO_0000203 NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP101458.RAaXa6RxqRbnXMScvC5ND6MsMSYc8RXA8W32LAg3y2SRM130_provenance.