Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- befree-2016 importedOn "2016-02-19" NP253471.RAqA6F_UlRMQKhyt1peqKrR6pfbXdkyRsCuSYXOojMLGk130_provenance.
- 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.