Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion> ?p ?o ?g. }
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- NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion type Assertion NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_head.
- NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion description "[Classic Bartter syndrome is due to a mutation in the gene encoding the chloride channel (CLCNKB), also a regulator of NKCC2, and typically presents in infancy or early childhood with failure to thrive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion evidence source_evidence_literature NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion SIO_000772 11780689 NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion wasDerivedFrom befree-20140225 NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_assertion wasGeneratedBy ECO_0000203 NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.