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- NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_assertion type Assertion NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_head.
- NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_assertion wasGeneratedBy ECO_0000203 NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_provenance.
- NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_assertion wasDerivedFrom befree-2016 NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_provenance.
- NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_assertion SIO_000772 10341296 NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_provenance.
- NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_assertion evidence source_evidence_literature NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_provenance.
- NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_assertion description "[Fragile X syndrome is the most common form of inherited mental retardation currently known, associated with a wide range of developmental disabilities in both males and females, caused by a large expansion of a (CGG)n repeat in the first exon of the FMR1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253472.RAnlzA-o0Rs647TLBhXIv5oCQDXv3XLqHuAEfR6ai578w130_provenance.