Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_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." NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_assertion evidence source_evidence_literature NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_assertion SIO_000772 11584361 NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_assertion wasDerivedFrom befree-20140225 NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_assertion wasGeneratedBy ECO_0000203 NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP646860.RAn4Mofd4l3-rAA3UrD-teOCt8yd90J6MPS1kMJ0zEP6I130_provenance.