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- source_evidence_literature type ECO_0000212 NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- befree-2016 importedOn "2016-02-19" NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion wasGeneratedBy ECO_0000203 NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion wasDerivedFrom befree-2016 NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion SIO_000772 18405873 NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion evidence source_evidence_literature NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.
- NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_assertion description "[Given its localization in both the Down syndrome critical region and in the minimal region for partial monosomy 21, the gene has been studied intensively in animals and in humans, and DYRK1A has been proposed to be involved in the neurodevelopmental alterations associated with these syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665338.RAbGOc8HHTncmEWe-inzC5Wral5A3V8G7LFnqTy9t4yQY130_provenance.