Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_assertion> ?p ?o ?g. }
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- NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_assertion type Assertion NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_head.
- NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_assertion description "[The expansion of CGG repeats in the 5'-untranslated region (5'UTR) of FMR1 gene is the molecular basis of fragile X syndrome in most of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_provenance.
- NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_assertion evidence source_evidence_literature NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_provenance.
- NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_assertion SIO_000772 21499798 NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_provenance.
- NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_assertion wasDerivedFrom befree-2016 NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_provenance.
- NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_assertion wasGeneratedBy ECO_0000203 NP887839.RAvGry4rXsBTwd-taVPIy6co0hixxKDJL3K6aFH8E71QE130_provenance.