Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_assertion description "[The inherited deficiencies of protein C, protein S, antithrombin III, factor V Leiden mutation, prothrombin gene polymorphism, and antiphospholipids were studied in 53 Budd-Chiari syndrome (BCS) and 33 portal vein thrombosis (PVT) cases and compared with 223 age- and sex-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_assertion evidence source_evidence_literature NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_assertion SIO_000772 11584361 NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_assertion wasDerivedFrom befree-20140225 NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_assertion wasGeneratedBy ECO_0000203 NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP926220.RA32Xs0HeQ_EiighvR3-2y3TqtZZ-LskczcJ8DeE6eq_o130_provenance.