Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_assertion> ?p ?o ?g. }
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- NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_assertion type Assertion NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_head.
- NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_assertion description "[Multiplex XLMR pedigrees have been reported with only one mutated patient having autism and MR: different X-located MR genes have been shown to be involved (NLGN4, MECP2, OPHN1, ZNF674 and FRAXA) which does not suggest that they could be autism genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_provenance.
- NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_assertion evidence source_evidence_literature NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_provenance.
- NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_assertion SIO_000772 19160128 NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_provenance.
- NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_assertion wasDerivedFrom befree-2016 NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_provenance.
- NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_assertion wasGeneratedBy ECO_0000203 NP715916.RAcs0rxxhvYhgOO61VR9tmS9o8DGcCGwvE3zadXh1TlGU130_provenance.