Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP651177.RAyDE7PL8v2kxMQioPbF-4rn0LlcXaMG6BK6C1oldD5qg130_provenance.