Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_assertion type Assertion NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_head.
- 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.
- NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_assertion evidence source_evidence_literature NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_provenance.
- NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_assertion SIO_000772 15629215 NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_provenance.
- NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_assertion wasDerivedFrom befree-20140225 NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_provenance.
- NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_assertion wasGeneratedBy ECO_0000203 NP485807.RAhYIr5-xfLl-z13SVzKqNWrsf6rf4jy9OKc9KKNSkYgQ130_provenance.