Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_assertion description "[Taken together with our recent findings of linkage between this region on chromosome 12 and an insulin-deficient form of NIDDM (NIDDM2), the data suggest that mutations at the MODY3/NIDDM2 gene(s) result in a reduced insulin secretory response, that subsequently progresses to diabetes and underlines the importance of subphenotypic classification in studies of diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_assertion evidence source_evidence_literature NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_assertion SIO_000772 9045858 NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_assertion wasDerivedFrom befree-20140225 NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_assertion wasGeneratedBy ECO_0000203 NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681271.RAI1vRGo9NCecpP5A-SBDH2tzPa3hfp4fDXIgzqrVQb94130_provenance.