Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion> ?p ?o ?g. }
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- NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion type Assertion NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_head.
- NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion description "[Heterozygous inactivating mutations of the calcium-sensing receptor (CaR) gene cause familial hypocalciuric hypercalcaemia (FHH), a generally benign disorder characterized by mild to moderate PTH-dependent hypercalcaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion evidence source_evidence_literature NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion SIO_000772 16649980 NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion wasDerivedFrom befree-20140225 NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_assertion wasGeneratedBy ECO_0000203 NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.