Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_assertion description "[Herein, we report that mutant huntingtin (mtHtt) induces the transcription of alpha thalassemia/mental retardation X linked (ATRX), an ATPase/helicase and SWI/SNF-like chromatin remodeling protein via Cdx-2 activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_assertion evidence source_evidence_literature NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_assertion SIO_000772 22240898 NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_assertion wasDerivedFrom befree-2016 NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_assertion wasGeneratedBy ECO_0000203 NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.
- befree-2016 importedOn "2016-02-19" NP952881.RApJVzuN3GO-ENX_WvVZ2AP4NpLaaedspQwevqdi9jyLw130_provenance.