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- source_evidence_literature type ECO_0000212 NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_assertion description "[However, among the subset of participants with red or blond hair, those with CMM were twice as likely to carry GSTM1 null (OR, 2.2; 95% CI, 1.2-4.2) and nearly 10-fold more likely to carry both GSTM1 null and GSTT1 null (OR, 9.5; 95% CI, 1.2-73) compared with those without CMM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_assertion evidence source_evidence_literature NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_assertion SIO_000772 11352862 NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_assertion wasDerivedFrom befree-20140225 NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_assertion wasGeneratedBy ECO_0000203 NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP251720.RAOpISx4pRKYJT4Sae9O9nso-IaLFVzYnhoQyJ-DBoC6c130_provenance.