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- NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_assertion type Assertion NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_head.
- NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_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." NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_provenance.
- NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_assertion evidence source_evidence_literature NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_provenance.
- NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_assertion SIO_000772 21633404 NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_provenance.
- NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_assertion wasDerivedFrom befree-2016 NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_provenance.
- NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_assertion wasGeneratedBy ECO_0000203 NP898771.RAFoxpf38pqHwzjhE_N80E4t073bdTh_vLtr9-7HEdvAs130_provenance.