Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_assertion description "[We identified interesting novel candidate genes that likely contribute to glioma progression and provide first evidence for a role of epigenetic silencing of AMOG in malignant glioma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_assertion evidence source_evidence_literature NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_assertion SIO_000772 16865689 NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_assertion wasDerivedFrom lhgdn-20090331 NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_assertion wasGeneratedBy ECO_0000203 NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP116798.RAXmwosXmaRSeSOh59c4g0Z6-S4MgfpbgXklEV0FHHEuY130_provenance.