Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_assertion description "[Functional characterization of calcium-sensing receptor codon 227 mutations presenting as either familial (benign) hypocalciuric hypercalcemia or neonatal hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_assertion evidence source_evidence_curated NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_assertion SIO_000772 15572418 NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_assertion wasDerivedFrom uniprot-20130724 NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_assertion wasGeneratedBy ECO_0000218 NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_provenance.