Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion description "[Aberrant differentiation in MDS can often be traced to abnormal DNA methylation (both gains and losses of DNA methylation genome wide and at specific loci) as well as mutations in genes that regulate epigenetic programs (TET2 and DNMT3a, both involved in DNA methylation control; EZH2 and ASXL1, both involved in histone methylation control).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion evidence source_evidence_literature NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion SIO_000772 23660859 NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion wasDerivedFrom befree-20140225 NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_assertion wasGeneratedBy ECO_0000203 NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP205994.RAHwYiggnKfIWDaHI6LYyFxCFZh4jE9_7CJOM9BRU2Xi0130_provenance.