Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_assertion description "[From a translational standpoint, hypermethylation can be used as a marker of recurrent disease or progression, for example, in MDS, or response to chemotherapy, such as MGMT methylation in B-cell non-Hodgkin's lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_assertion evidence source_evidence_literature NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_assertion SIO_000772 14585279 NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_assertion wasDerivedFrom befree-2016 NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_assertion wasGeneratedBy ECO_0000203 NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.
- befree-2016 importedOn "2016-02-19" NP418694.RAqw_oINF-hAvlb0bsgbDvMWLeMWC-UQfmnBua99tlbKc130_provenance.