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- NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_assertion type Assertion NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_head.
- NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_assertion wasGeneratedBy ECO_0000203 NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_assertion wasDerivedFrom befree-2016 NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_assertion SIO_000772 10341296 NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_assertion evidence source_evidence_literature NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_assertion description "[The fragile X syndrome is due to the shutdown of the FMR1 gene transcription, and the pathogenesis of this syndrome is a consequence of absence of the protein product of the FMR1 gene (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.