Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_assertion description "[Furthermore, in a cross-sectional study among patients with IgA-GN, a logistic regression model showed that the risk for homozygous DD was greater, although not at a statistically significant level in the end-stage renal failure subgroup compared with the normal renal function subgroup (odds ratio = 3.16; CI, 0.7 to 13.7) after adjustment by sex, age at biopsy, HPT, PTO, and therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_assertion evidence source_evidence_literature NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_assertion SIO_000772 10352195 NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_assertion wasDerivedFrom befree-20140225 NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_assertion wasGeneratedBy ECO_0000203 NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP383739.RAKa0pD7KiFkjmH4RisnXeeGgInit_HHz3ofwXXffw3v8130_provenance.