Matches in Nanopublications for { ?s ?p "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP126994.RANKZEpiUi2zTp5TG0AWi0VjG5txs1aQ4VPKZJhY2FcLw130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP126994.RANKZEpiUi2zTp5TG0AWi0VjG5txs1aQ4VPKZJhY2FcLw130_provenance.
- NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136868.RAi9EjqxPHaOXE4oN1YmdujqG5RQxXvqb_JnVSlAdbZ_k130_provenance.
- NP124228.RA1qNFLUmzZlFlis9dtDHUwTBMcE39s-hTjDQe5Y_dVLU130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124228.RA1qNFLUmzZlFlis9dtDHUwTBMcE39s-hTjDQe5Y_dVLU130_provenance.
- NP207411.RAwdb3HXGVCA3gdLBG89P67Lc1Mkyn7XemiCXoTNhqfTY130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207411.RAwdb3HXGVCA3gdLBG89P67Lc1Mkyn7XemiCXoTNhqfTY130_provenance.
- NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_provenance.
- NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200019.RAP9Vfg5Vs2zZgyDbgWXykz5rS1Ey1H3PbIKeL3i28hU4130_provenance.
- assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP187413.RAu56Kfrhl_WYLC9Rg9RsHTdVWddOGGz5g4dNk1pEHCsk130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187413.RAu56Kfrhl_WYLC9Rg9RsHTdVWddOGGz5g4dNk1pEHCsk130_provenance.
- NP190175.RAu7CbOKQNdT__N7tHJbKjgX4BeSUg-sdZfXkPWAHk53U130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190175.RAu7CbOKQNdT__N7tHJbKjgX4BeSUg-sdZfXkPWAHk53U130_provenance.
- assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP207413.RAOApEIZJ6lNnKgN6KaP_cwgOn0GDfaJgPoz34E-nrAwY130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207413.RAOApEIZJ6lNnKgN6KaP_cwgOn0GDfaJgPoz34E-nrAwY130_provenance.