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- source_evidence_literature type ECO_0000212 NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion description "[Until recently, HI was generally considered an orphan disease, but as parallel defects in ion channels, enzymes, and metabolic pathways also give rise to diabetes and impaired insulin release, the HI paradigm has wider implications for more common disorders of the endocrine pancreas and the molecular physiology of ion transport.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion evidence source_evidence_literature NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion SIO_000772 14715916 NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion wasDerivedFrom befree-2016 NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_assertion wasGeneratedBy ECO_0000203 NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.
- befree-2016 importedOn "2016-02-19" NP427515.RAMkAL3La6wgkSniJI_AMKoxsWvbUSpvYYtlbXY1aQHqw130_provenance.