Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_assertion description "[Disorders of the DNA methylation machinery include both the aforementioned writers and also the readers of the methyl mark, such as MeCP2, the cause of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_assertion evidence source_evidence_literature NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_assertion SIO_000772 25192503 NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_assertion wasDerivedFrom befree-2016 NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_assertion wasGeneratedBy ECO_0000203 NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217261.RAwOgo8sbCQgtp2G_D6jP1k_WO0Ott3BzPbCmspNvstuM130_provenance.