Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_assertion> ?p ?o ?g. }
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- NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_assertion type Assertion NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_head.
- NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_assertion description "[Deficient transcriptional initiation, and not elongation, is the major cause of FXN transcriptional deficiency in FRDA, and it is related to the spread of repressive chromatin from the expanded GAA-TR mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_provenance.
- NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_assertion evidence source_evidence_literature NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_provenance.
- NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_assertion SIO_000772 24737321 NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_provenance.
- NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_assertion wasDerivedFrom befree-20150227 NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_provenance.
- NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_assertion wasGeneratedBy ECO_0000203 NP411403.RAe0hFH6G8fd5w-CPCMYhlJRWKqJauEXjtRijqroXNI58130_provenance.