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- source_evidence_literature type ECO_0000212 NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_assertion description "[Single-SNP analysis demonstrated significant associations of the CARD15_R702W variation and the NALP12_In9 T-allele with AD (P = 0.008 and P = 0.03, resp.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_assertion evidence source_evidence_literature NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_assertion SIO_000772 17620097 NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_assertion wasDerivedFrom befree-20140225 NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_assertion wasGeneratedBy ECO_0000203 NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP369487.RAl2EN_rewWl20oUlTaYRF0K3G8nkmCmp2ckPHKdTHKm8130_provenance.