Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion wasGeneratedBy ECO_0000203 NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion wasDerivedFrom befree-2016 NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion SIO_000772 23637977 NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion evidence source_evidence_literature NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.
- NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_assertion description "[Although none of the association p-values were statistically significant after adjustment for multiple comparisons, SNPs in CYP1B1 were strongly associated with KIT exon 11 codon 557-8 deletions (OR = 1.9, 95% CI: 1.3-2.9 for rs2855658 and OR = 1.8, 95% CI: 1.2-2.7 for rs1056836) and wild type GISTs (OR = 2.7, 95% CI: 1.5-4.8 for rs1800440 and OR = 0.5, 95% CI: 0.3-0.9 for rs1056836).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1074396.RA0umR98dvQXvZYwgCgPvRrLeJ1_TWNPqUADW5_RKJpP0130_provenance.