Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- befree-2016 importedOn "2016-02-19" NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_assertion wasGeneratedBy ECO_0000203 NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_assertion wasDerivedFrom befree-2016 NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_assertion SIO_000772 15579781 NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_assertion evidence source_evidence_literature NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.
- NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_assertion description "[We selected 15 hyperinsulinism of infancy patients and systematically sequenced the promoter and all coding exons and intron/exon boundaries of ABCC8 and KCNJ11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471298.RAulHvQEf15sCXNY5WZaF2yPLF0N6hXh8Eb0stBc_WRtk130_provenance.