Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_assertion description "[We identified genetic associations between Behcet's disease and single-nucleotide polymorphisms (SNPs) in KIAA1529, CPVL, LOC100129342, UBASH3B, and UBAC2 (odds ratio = 2.04, 2.26, 1.84, 1.71, and 1.61, respectively; P value = 4.2 x 10-5, 1.0 x 10-4, 3.0 x 10-4, 1.5 x 10-3, and 5.8 x 10-3, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_assertion evidence source_evidence_literature NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_assertion SIO_000772 19442274 NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_assertion wasDerivedFrom gad-20150221 NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_assertion wasGeneratedBy ECO_0000203 NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP147401.RAnb_Py6f56L9Cqj_lS5TglbowLRVx7xj-5j6Xmp9nVh8130_provenance.