Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_assertion description "[A gene (NPH1) responsible for approximately 90% of the purely renal form of familial juvenile nephronophthisis, a progressive tubulo-interstitial kidney disorder, maps to human chromosome 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_assertion evidence source_evidence_literature NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_assertion SIO_000772 8825638 NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_assertion wasDerivedFrom befree-20140225 NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_assertion wasGeneratedBy ECO_0000203 NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.
- befree-20140225 importedOn "2014-02-25" NP647183.RAAuviww2WKsW2M4Xg-kBODriRVcufAgnACswnJ8pbnik130_provenance.