Matches in Nanopublications for { ?s ?p "[Recently, the FOXG1 gene was implicated in the molecular aetiology of the congenital variant of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_assertion description "[Recently, the FOXG1 gene was implicated in the molecular aetiology of the congenital variant of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237618.RAeKKhlSGxZsyzVBmR606sRTaV59YsNNAd9J74Ngnm3ik130_provenance.
- assertion description "[Recently, the FOXG1 gene was implicated in the molecular aetiology of the congenital variant of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP767577.RACUUAu3GGuNC_J7cRSuuofG9Lf6Kh-8zhkfHuWl_h2hI130_assertion description "[Recently, the FOXG1 gene was implicated in the molecular aetiology of the congenital variant of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767577.RACUUAu3GGuNC_J7cRSuuofG9Lf6Kh-8zhkfHuWl_h2hI130_provenance.
- NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_assertion description "[Recently, the FOXG1 gene was implicated in the molecular aetiology of the congenital variant of Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404359.RA4tN4dtkkCbswoRcko50VFPVOR0dM0ptUMQxqMUcvv-c130_provenance.