Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_assertion description "[Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_assertion evidence source_evidence_curated NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_assertion SIO_000772 12761627 NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_assertion wasDerivedFrom uniprot-20130724 NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_assertion wasGeneratedBy ECO_0000218 NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP809.RAFv6zm5KLXG3JgsT9YbQKATl0J5FLkjzLfdpE_H4WLmQ130_provenance.