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- source_evidence_literature type ECO_0000212 NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_assertion description "[In conclusion, this case report of MEN 2A linked to a 634 RET mutation was peculiar by its revelation mode (1) hyperparathyroidism moreover linked to an adenoma and (2) associated with diabetes, mechanisms of which are probably multifactorial (familial type 2 diabetes, hypercalcemia, catecholamines excess).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_assertion evidence source_evidence_literature NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_assertion SIO_000772 18752792 NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_assertion wasDerivedFrom befree-20150227 NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_assertion wasGeneratedBy ECO_0000203 NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP670705.RAguPpK1DAvHlb7a-9GTKQl5D1Q3W9lvAic_VGCpADl2k130_provenance.