Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- NP723199.RA2ROeR6FJt8-ZOh9PGLSLUYTs9RBqyNuZMIS-ZxCdWPg130_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." NP723199.RA2ROeR6FJt8-ZOh9PGLSLUYTs9RBqyNuZMIS-ZxCdWPg130_provenance.
- NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_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." NP723200.RA7pz1NJvd9av2MZZbtY3AB1oaVDvtLra3bOf2JT32-Ho130_provenance.
- 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." provenance.
- 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." provenance.
- NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_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." NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_provenance.