Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_assertion description "[In FSHD, the combination of inefficient chromatin silencing of the D4Z4 repeat and polymorphisms on the FSHD-permissive alleles that stabilize the DUX4 mRNAs emanating from the repeat result in inappropriate DUX4 protein expression in muscle cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_assertion evidence source_evidence_literature NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_assertion SIO_000772 21288772 NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_assertion wasDerivedFrom befree-20140225 NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_assertion wasGeneratedBy ECO_0000203 NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP198835.RAKB7NdFRIfTziZRkgPvNSTSTbFa8jXdASddJQkDVG-Wo130_provenance.