Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_assertion> ?p ?o ?g. }
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- NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_assertion type Assertion NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_head.
- NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_assertion description "[The molecular mechanism of the fragile X syndrome is based on the expansion of an CGG repeat in the 5' UTR of the FMR1 gene in the majority of fragile X patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_provenance.
- NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_assertion evidence source_evidence_literature NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_provenance.
- NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_assertion SIO_000772 7668289 NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_provenance.
- NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_assertion wasDerivedFrom befree-20140225 NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_provenance.
- NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_assertion wasGeneratedBy ECO_0000203 NP529658.RAdNYh8-LTypiCvbRztHDttdWO_cKqdrUHeb-ZW8R29B4130_provenance.