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- source_evidence_literature type ECO_0000212 NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_assertion description "[The most common inherited traits (deficiency in antithrombin, protein C, or protein S, factor V Leiden, prothrombin G20210A) and mild hyperhomocysteinemia are diagnosed in at least 40% of patients with venous thromboembolism (VTE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_assertion evidence source_evidence_literature NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_assertion SIO_000772 12368166 NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_assertion wasDerivedFrom befree-20140225 NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_assertion wasGeneratedBy ECO_0000203 NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP786403.RAPS6Uqc_0n0DPqS6K8G-2_Lk5GS0PS2p-AjrA9PjyvoM130_provenance.