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- source_evidence_literature type ECO_0000212 NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_assertion description "[Mutations in the 11beta-HSD2 gene cause a rare form of inherited hypertension, the syndrome of apparent mineralocorticoid excess (AME), in which cortisol activates the MR resulting in severe hypertension and hypokalemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_assertion evidence source_evidence_literature NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_assertion SIO_000772 16980198 NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_assertion wasDerivedFrom befree-2016 NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_assertion wasGeneratedBy ECO_0000203 NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.
- befree-2016 importedOn "2016-02-19" NP569653.RAig44aKU-I3NJulm7k2J4kfnTOToDnNFrKQ9MiOkP-ig130_provenance.