Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_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." NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_assertion evidence source_evidence_literature NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_assertion SIO_000772 22240898 NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_assertion wasDerivedFrom befree-20150227 NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_assertion wasGeneratedBy ECO_0000203 NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP308955.RAT2OSt5sMcmkIWZf3f6Q0fcJ66Q39rpFtUKw5tcKFiE0130_provenance.