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- source_evidence_literature type ECO_0000212 NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_assertion description "[The C allele at SNP rs806365 (frequency, 57.4%), ~4.1 kb 3' from CNR1, was associated with increased HOMA(IR) (n = 2,261, ? = 0.05 per C, empirical P = 0.01), risk of T2D (674 cases, odds ratio = 1.19 per C, nominal P = 0.01) and CHD (237 cases, hazard ratio = 1.23 per C, nominal P = 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_assertion evidence source_evidence_literature NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_assertion SIO_000772 21633404 NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_assertion wasDerivedFrom befree-20150227 NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_assertion wasGeneratedBy ECO_0000203 NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.
- befree-20150227 importedOn "2015-02-27" NP318520.RA-SXPJwSU6jHchaK3GZkjNoGe7SfqL6gAVvltNDkoV68130_provenance.