Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_assertion description "[The frequency of either the FVL or prothrombin sequence variant was not increased in idiopathic PE patients compared with nonidiopathic PE patients or patients who had PE excluded.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_assertion evidence source_evidence_literature NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_assertion SIO_000772 16574759 NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_assertion wasDerivedFrom gad-20150221 NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_assertion wasGeneratedBy ECO_0000203 NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.
- gad-20150221 importedOn "2015-02-21" NP130871.RATbL8g6SucTOM5i2tKcAFSUfK_NYNE6amCbT30aOLQ54130_provenance.