Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_assertion type Assertion NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_head.
- NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_assertion wasGeneratedBy ECO_0000203 NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_provenance.
- NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_assertion wasDerivedFrom befree-20150227 NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_provenance.
- NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_assertion SIO_000772 7888141 NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_provenance.
- NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_assertion evidence source_evidence_literature NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_provenance.
- NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_assertion description "[The findings in the present family illustrate that the typical characteristics of the fragile X syndrome can be caused by other types of mutations involving the FMR1 than the highly expanded stretches of CGG repeats in the 5' noncoding region of the FMR1 gene, coinciding with abnormal methylation patterns in that area as present in the vast majority of individuals with the fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408921.RALI3N9cdNnELp5cxpKy_TcSDUDBzuPOecAUa6tRQ6ygM130_provenance.