Matches in Nanopublications for { ?s ?p "[Fragile X syndrome is a neurodevelopmental disorder that is caused by large methylated expansions of a CGG repeat (>200) region upstream of the FMR1 gene that results in the lack of expression of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_assertion description "[Fragile X syndrome is a neurodevelopmental disorder that is caused by large methylated expansions of a CGG repeat (>200) region upstream of the FMR1 gene that results in the lack of expression of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_provenance.
- NP599360.RA4iVplQiB2uATGF_vy9XpX3t1sF8i7tOlUPHzROKuH-Y130_assertion description "[Fragile X syndrome is a neurodevelopmental disorder that is caused by large methylated expansions of a CGG repeat (>200) region upstream of the FMR1 gene that results in the lack of expression of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599360.RA4iVplQiB2uATGF_vy9XpX3t1sF8i7tOlUPHzROKuH-Y130_provenance.
- NP914274.RAHMzaqmqzHJ2GTm3c5YU8WEizwkhvXk9aae2HF7ZLRMg130_assertion description "[Fragile X syndrome is a neurodevelopmental disorder that is caused by large methylated expansions of a CGG repeat (>200) region upstream of the FMR1 gene that results in the lack of expression of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914274.RAHMzaqmqzHJ2GTm3c5YU8WEizwkhvXk9aae2HF7ZLRMg130_provenance.