Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_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." NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_assertion evidence source_evidence_literature NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_assertion SIO_000772 22240898 NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_assertion wasDerivedFrom befree-20140225 NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_assertion wasGeneratedBy ECO_0000203 NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP895025.RAgnL5JkAjytuVZtrjgPkVukN3G3LzusqikCS8G2i_1w0130_provenance.