Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_assertion description "[All participants had a thrombotic workup that included the following: genetic markers: factor V Leiden G1691A and G20210A prothrombin mutations, methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms; protein assays: protein C, protein S and antithrombin; other tests: blood typing and screening for hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_assertion evidence source_evidence_literature NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_assertion SIO_000772 23337711 NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_assertion wasDerivedFrom befree-20140225 NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_assertion wasGeneratedBy ECO_0000203 NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP746538.RADSjr-g1xopDPkca-bwIuSwTIGsDkqPusWV_y2bpeo7U130_provenance.