Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_assertion description "[In conclusion, a silent polymorphism in exon 18 of the SUR1 gene is associated with NIDDM in a Danish Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_assertion evidence source_evidence_literature NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_assertion SIO_000772 9568693 NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_assertion wasDerivedFrom befree-2016 NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_assertion wasGeneratedBy ECO_0000203 NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1394195.RACFBmQaNSo1zkid0sFuphfJqk2MdL_Y4CcstZbhOJwlY130_provenance.