Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_assertion description "[Two men with this condition, a 56 year old and a 31 year old presenting with acute SMVT, demonstrated on CT scan, were subjected to a thrombophilia screen consisting of Protein C, S, antithrombin levels, lupus anticoagulant, anticardiolipin antibodies, fibrinogen levels, factor VIII levels, factor V 'Leiden' gene mutation, and paroxysmal nocturnal hematuria screen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_assertion evidence source_evidence_literature NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_assertion SIO_000772 15266932 NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_assertion wasDerivedFrom befree-2016 NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_assertion wasGeneratedBy ECO_0000203 NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP452911.RARdqJdackSGkzpXCNjmC0O3f-JEKM2OVgPZQWaHlUzCQ130_provenance.