Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_assertion description "[However, the frequency distribution of KLK1 promoter among VUR patients with or without CRI (A, 50.0% and 67.5%; B, 17.9% and 8.3%; H, 14.3% and 18.3%; K, 17.9% and 5.8%, respectively) was statistically different (P = 0.008).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_assertion evidence source_evidence_literature NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_assertion SIO_000772 15086490 NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_assertion wasDerivedFrom befree-20140225 NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_assertion wasGeneratedBy ECO_0000203 NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213591.RAuNYFffLHR2PmzY8l7CB-TvrCSA3wbFeBUdRL9szDQ20130_provenance.