Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_assertion> ?p ?o ?g. }
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- NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_assertion type Assertion NP920.RALLCn1TDbVMyLxScRC5N-TfFmLH9GrbriWFHTJ2k6J9A130_head.
- 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.