Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_assertion description "[In metabolic studies patient exhibited abnormalities similar to those reported in Bartter's syndrome; viz, hypokalemic alkalosis, blunted response to exogenous angiotensin II, which reverted to normal by volume expansion with an albumin solution, and diminished fractional free water clearance per fractional distal sodium delivery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_assertion evidence source_evidence_curated NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_assertion SIO_000772 7182184 NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_assertion wasDerivedFrom ctd_human-20130708 NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_assertion wasGeneratedBy ECO_0000218 NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP7933.RAyFy3UL3H3UrsgHces0zctluW9XuJvTi9AW0Gx7ylcoY130_provenance.