Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_assertion description "[Altered expression of several mental retardation genes such as UBE3A (Angelman Syndrome), ZEB2 (Mowat-Wilson Syndrome) and MEF2C was also found in TCF4-depleted cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_assertion evidence source_evidence_literature NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_assertion SIO_000772 24058414 NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_assertion wasDerivedFrom befree-2016 NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_assertion wasGeneratedBy ECO_0000203 NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.
- befree-2016 importedOn "2016-02-19" NP1112753.RAm97XTHv7EQCV1GmFzSrIRu21RCDK9_M7q6BrTifgsko130_provenance.