Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_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." NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_assertion evidence source_evidence_literature NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_assertion SIO_000772 24148886 NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_assertion wasDerivedFrom befree-2016 NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_assertion wasGeneratedBy ECO_0000203 NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1121630.RARFJdHF2K9FIJQ1qsb-7yBAj4QI1Uxs95EvMjkTQOajk130_provenance.