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- source_evidence_literature type ECO_0000212 NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_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." NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_assertion evidence source_evidence_literature NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_assertion SIO_000772 9045858 NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_assertion wasDerivedFrom befree-20150227 NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_assertion wasGeneratedBy ECO_0000203 NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP591707.RAThBl_1RAWhjNxJpOCoc7yv4m2JMHX7gjjv36fsEJWJg130_provenance.