Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_assertion> ?p ?o ?g. }
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- NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_assertion type Assertion NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_head.
- NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_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." NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_provenance.
- NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_assertion evidence source_evidence_literature NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_provenance.
- NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_assertion SIO_000772 12368166 NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_provenance.
- NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_assertion wasDerivedFrom befree-20140225 NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_provenance.
- NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_assertion wasGeneratedBy ECO_0000203 NP337235.RAwvQx14CjKAkRR4Lep_OqhfZSwnnThRZi9BrRzXv8MBI130_provenance.