Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_assertion> ?p ?o ?g. }
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- NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_assertion type Assertion NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_head.
- NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_assertion wasGeneratedBy ECO_0000203 NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_provenance.
- NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_assertion wasDerivedFrom befree-20150227 NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_provenance.
- NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_assertion SIO_000772 19251738 NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_provenance.
- NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_assertion evidence source_evidence_literature NP919592.RAv9yy9SOJVrZDIRVDUXdZRn3aj2lF48YEeHHdNmqeWv8130_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.