Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_assertion description "[This AIR pattern suggested a K(ATP) channel defect because it resembled that seen in children with recessive hyperinsulinism due to two common SUR1 mutations, g3992-9a and delPhe1388.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_assertion evidence source_evidence_literature NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_assertion SIO_000772 12941782 NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_assertion wasDerivedFrom befree-2016 NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_assertion wasGeneratedBy ECO_0000203 NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.
- befree-2016 importedOn "2016-02-19" NP406838.RAgs-2TglxAdjiHQ2_MruTKmxEih-HSNc4E4FHhIJbEOY130_provenance.