Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_assertion description "[Infrequent miR-124-1 methylation detected in diagnostic and relapse MM samples showed an unimportant role in MM pathogenesis, despite frequent methylation found in cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_assertion evidence source_evidence_literature NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_assertion SIO_000772 21544199 NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_assertion wasDerivedFrom befree-2016 NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_assertion wasGeneratedBy ECO_0000203 NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.
- befree-2016 importedOn "2016-02-19" NP891838.RAxrQTgxJ2FxU94T0L3nGgxwIaX9VMV1eCFLJEIJngLFY130_provenance.