Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_assertion description "[However, the ubiquity, extent, and correlation with disease progression suggest that aberrant DNA methylation is the dominant mechanism for TSG silencing and clonal variation in MDS evolution to AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_assertion evidence source_evidence_literature NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_assertion SIO_000772 18832655 NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_assertion wasDerivedFrom befree-20140225 NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_assertion wasGeneratedBy ECO_0000203 NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP817744.RAWlXBD1ds07IK7qCNthS9nwDchSx8tOr-imFMKCw-Yfs130_provenance.