Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_assertion description "[Congenital nephrogenic diabetes insipidus (NDI) is a rare disease caused most often by mutations in the vasopressin V2 receptor (AVPR2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_assertion evidence source_evidence_literature NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_assertion SIO_000772 9302264 NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_assertion wasDerivedFrom befree-20140225 NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_assertion wasGeneratedBy ECO_0000203 NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900024.RAfN0Xc3WN9GAZceldh2Kvff5qycWskO1Aq9RUTRIRY68130_provenance.