Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_assertion description "[We identified genetic associations between Beh�et'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." NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_assertion evidence source_evidence_literature NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_assertion SIO_000772 19442274 NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_assertion wasDerivedFrom befree-2016 NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_assertion wasGeneratedBy ECO_0000203 NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.
- befree-2016 importedOn "2016-02-19" NP738982.RAs6LdqcHNBufoc8Qdt-PMiGBPFDs-EsJwtiW54K5D9Ok130_provenance.