Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_assertion description "[A combination of the methylation status of HOXA9 and EN1 could discriminate HGSOC from benign OSE with a sensitivity of 98.8% and a specificity of 91.7%, which increased to 100% sensitivity with no loss of specificity when pre-operative CA125 levels were also incorporated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_assertion evidence source_evidence_literature NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_assertion SIO_000772 22115852 NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_assertion wasDerivedFrom befree-20140225 NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_assertion wasGeneratedBy ECO_0000203 NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP326156.RAeTf96JI8JBsm-EjRnhTf7QfDRfvVzhyLbQhc7jgFHz8130_provenance.