Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_assertion description "[In gain-of-function CaSR mutations, the genetic abnormalities increase CaSR activity leading to the development of such clinical manifestations as hypercalciuric hypocalcemia and hypoparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_assertion evidence source_evidence_literature NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_assertion SIO_000772 15960151 NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_assertion wasDerivedFrom lhgdn-20090331 NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_assertion wasGeneratedBy ECO_0000203 NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211491.RAVuf7EoOHBPNFx8HCXfuGkC0vmDkUCGu7ZgODFYtazWM130_provenance.