Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_assertion description "[When WT1 Ab was combined with CEA or CYFRA for detection of NSCLC, positive detection rates increased from 25.0 to 34.1 and 31.8%, respectively, in stage I and from 38.4 to 69.2 and 46.1%, respectively, in stage III, but not changed in stage II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_assertion evidence source_evidence_literature NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_assertion SIO_000772 19384943 NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_assertion wasDerivedFrom befree-2016 NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_assertion wasGeneratedBy ECO_0000203 NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.
- befree-2016 importedOn "2016-02-19" NP733990.RAeMSy6_PXdUpQA4ByTWaidiUH37RVldFrwXV9RZyu8Cc130_provenance.