Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_assertion description "[Mutations in AQP2 cause autosomal nephrogenic diabetes insipidus (NDI), a disease that renders the kidney unresponsive to vasopressin, resulting in polyuria and polydipsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_assertion evidence source_evidence_literature NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_assertion SIO_000772 19701945 NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_assertion wasDerivedFrom befree-20140225 NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_assertion wasGeneratedBy ECO_0000203 NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP588896.RA8wOHC9sehPY6vPCf8KcHu_GmkGC9dkwEAeHGCFWeKkM130_provenance.