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- source_evidence_literature type ECO_0000212 NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_assertion description "[This study has identified a strong and repeated association between the AGTR1 1166C allele and susceptibility to AAA, and a weaker effect associated with the ACE deletion allele, in 3 geographically distinct, but ethnically similar, case-control cohorts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_assertion evidence source_evidence_literature NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_assertion SIO_000772 18239157 NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_assertion wasDerivedFrom befree-20140225 NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_assertion wasGeneratedBy ECO_0000203 NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212370.RA96Qyoi19ETpCh3vGltgYqcnf2eajCKYd-iaQOxOwADE130_provenance.