Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_assertion> ?p ?o ?g. }
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- NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_assertion type Assertion NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_head.
- NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_assertion description "[Fragile X syndrome (FXS), the most-frequently inherited form of intellectual disability and the most-prevalent single-gene cause of autism, results from a lack of fragile X mental retardation protein (FMRP), an RNA-binding protein that acts, in most cases, to repress translation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_provenance.
- NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_assertion evidence source_evidence_literature NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_provenance.
- NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_assertion SIO_000772 26350240 NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_provenance.
- NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_assertion wasDerivedFrom befree-2016 NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_provenance.
- NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_assertion wasGeneratedBy ECO_0000203 NP1293848.RAd2mLYeolclEceaqXamm5xy5k4l9gZdbHtUc3YfPWvDg130_provenance.