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- source_evidence_literature type ECO_0000212 NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_assertion description "[The preliminary results obtained in this study revealed an association of the MTHFR and APOE gene polymorphism with cerebrovascular disease, suggesting a significant risk for stroke in subjects who are homozygous for the T allele and for carotid stenosis in subjects having APOEepsilon3epsilon4 genotype. Additional studies in larger patient groups are needed to confirm these observations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_assertion evidence source_evidence_literature NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_assertion SIO_000772 11388660 NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_assertion wasDerivedFrom gad-20130706 NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_assertion wasGeneratedBy ECO_0000203 NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP61489.RAlXbAuH0bPlHkdx4M6tIcIkf2u-rvYhF-sNgJX8z3xd0130_provenance.