Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_assertion description "[In summary, a CDH2 promoter polymorphism influences the risk of OA, and hnRNP K was found to be involved in the regulation of elevated N-cadherin expression in patients with OA carrying the minor allele of rs11564299.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_assertion evidence source_evidence_literature NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_assertion SIO_000772 24148886 NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_assertion wasDerivedFrom befree-20150227 NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_assertion wasGeneratedBy ECO_0000203 NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.
- befree-20150227 importedOn "2015-02-27" NP461963.RAR3NTjDLYcaFiGqJU3Cq6IcdRS-z_-08FG1nOm9S6Rng130_provenance.