Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_assertion> ?p ?o ?g. }
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- NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_assertion type Assertion NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_head.
- NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_assertion description "[Here we describe an additional LND female, who presented with acute renal failure at the age of two months, in whom absence of transcription of the two HPRT alleles occurred due to as yet undescribed mechanism in LND females: the transcription of one HPRT allele was blocked due to a de novo X chromosome-autosome translocation 46,XX,t(X:2)(q26:p25), with a breaking point encompassing the HPRT gene locus, whereas the transcription of the normal allele was inhibited due to non-random inactivation of the second X-chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_provenance.
- NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_assertion evidence source_evidence_literature NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_provenance.
- NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_assertion SIO_000772 16343967 NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_provenance.
- NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_assertion wasDerivedFrom befree-20140225 NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_provenance.
- NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_assertion wasGeneratedBy ECO_0000203 NP811621.RAOxJd4mBxIoYOqaY6FXdx-dvh-g4p701xWTvJe9oQt78130_provenance.