Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_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." NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_assertion evidence source_evidence_literature NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_assertion SIO_000772 15086490 NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_assertion wasDerivedFrom befree-2016 NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_assertion wasGeneratedBy ECO_0000203 NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP440087.RARJ8KNKPf2nFlauKQkB6FqRLPCBexPWxaF7xIrcw-i6Q130_provenance.