Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_assertion description "[Autosomal dominant hypocalcemia (ADH) caused by activating mutations of calcium-sensing receptor (CaSR) is characterized by hypocalcemia with inappropriately low concentration of PTH and relative hypercalciuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_assertion evidence source_evidence_literature NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_assertion SIO_000772 12733714 NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_assertion wasDerivedFrom befree-20150227 NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_assertion wasGeneratedBy ECO_0000203 NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP972549.RANnGswhf_eG4g5evHBPfaIrMW1qJtbBnwt2xgNVh4Aqk130_provenance.