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- source_evidence_literature type ECO_0000212 NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP323738.RAZWkFk5LbKROE3lUa4tVa-py4yo0Ocn8p1xrQZetRykE130_provenance.