Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_assertion> ?p ?o ?g. }
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- NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_assertion type Assertion NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_head.
- NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_assertion description "[The mislocalization of CLC-K2 was identified as the molecular pathogenesis of Bartter syndrome by mutant barttins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_provenance.
- NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_assertion evidence source_evidence_literature NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_provenance.
- NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_assertion SIO_000772 12761627 NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_provenance.
- NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_assertion wasDerivedFrom lhgdn-20090331 NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_provenance.
- NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_assertion wasGeneratedBy ECO_0000203 NP149991.RAhpP8tLrx4cBlVCkGgFRFYWMxpxa6rZeAa88ehopCn7Q130_provenance.