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- source_evidence_literature type ECO_0000212 NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_assertion description "[With the aim of establishing whether the HR2 haplotype in factor V affects the risk of venous thromboembolism, a retrospective multicenter cohort study was performed in 810 family members identified through 174 probands who suffered from at least 1 episode of deep vein thrombosis and/or pulmonary embolism and had an inherited defect associated with thrombophilia (antithrombin, protein C, or protein S deficiency; factor V R506Q or prothrombin G20210A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_assertion evidence source_evidence_literature NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_assertion SIO_000772 10556190 NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_assertion wasDerivedFrom befree-20140225 NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_assertion wasGeneratedBy ECO_0000203 NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP312652.RA8AECoctKnzdSq9u8ANXl4nocQcL6_wM4Fz-OuwIeTjM130_provenance.