Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_assertion> ?p ?o ?g. }
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- NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_assertion type Assertion NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_head.
- NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_assertion description "[Smaller, so-called premutation expansions (55-200 repeats) can cause a family of neurodevelopmental phenotypes (attention deficit hyperactivity disorder, autism spectrum disorder, seizure disorder) and neurodegenerative (fragile X-associated tremor/ataxia syndrome [FXTAS]) phenotypes through an entirely distinct molecular mechanism involving increased FMR1 mRNA production and toxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_provenance.
- NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_assertion evidence source_evidence_literature NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_provenance.
- NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_assertion SIO_000772 23867198 NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_provenance.
- NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_assertion wasDerivedFrom befree-20140225 NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_provenance.
- NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_assertion wasGeneratedBy ECO_0000203 NP610688.RAbR8AWOzftOS0SH13Gg99PD8zMh6gbKYe9I4zxq7l7-o130_provenance.