Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_assertion> ?p ?o ?g. }
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- NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_assertion type Assertion NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_head.
- NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_assertion wasGeneratedBy ECO_0000203 NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_provenance.
- NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_assertion wasDerivedFrom befree-20140225 NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_provenance.
- NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_assertion SIO_000772 19251738 NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_provenance.
- NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_assertion evidence source_evidence_literature NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_provenance.
- NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_assertion description "[These features are similar to those of gene enhancer elements, raising the possibility that CHD7 functions in enhancer mediated transcription, and that the congenital anomalies in CHARGE syndrome are due to alterations in transcription of tissue-specific genes normally regulated by CHD7 during development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222707.RAz2dZhlqG0OjCZT1Fxpb6gP0v210VOTw9EiIMvVVe8oo130_provenance.