Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_assertion> ?p ?o ?g. }
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- NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_assertion type Assertion NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_head.
- NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_assertion wasGeneratedBy ECO_0000203 NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_provenance.
- NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_assertion wasDerivedFrom befree-2016 NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_provenance.
- NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_assertion SIO_000772 9211186 NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_provenance.
- NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_assertion evidence source_evidence_literature NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_provenance.
- NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_assertion description "[The fragile X syndrome is caused by the amplification of a polymorphic CGG repeat in the 5' untranslated region of the FMR1 gene and is the most common form of inherited mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376231.RA12hu9uDL5av3TSsLDHqCDED6yFB3NAVgggIWpl9kxt4130_provenance.