Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion description "[Genetic evidence suggests their involvement in transepithelial transport of chloride in distal nephron segments; ClC-K1 gene deletion leads to nephrogenic diabetes insipidus in mice, and mutations of the hClC-Kb gene cause Bartter's syndrome type III in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion evidence source_evidence_literature NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion SIO_000772 10831588 NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion wasDerivedFrom befree-20150227 NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_assertion wasGeneratedBy ECO_0000203 NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP315491.RAkUNVU9gb7FnOgLmzmscuU6zqxyUUohnGjv0Y2EAbLwQ130_provenance.