Matches in Nanopublications for { ?s ?p "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP557120.RAcqvnlTPH4BCqKtJ93F_kqeEmpyrWcJJEPLzQPU_zaf0130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557120.RAcqvnlTPH4BCqKtJ93F_kqeEmpyrWcJJEPLzQPU_zaf0130_provenance.
- NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552018.RAtZX8R-tsBTLCZxkflSsrhWzSwJ0UsimqeF8FJFrdDjk130_provenance.
- NP557115.RA6r3eW66pd9Jyx322yNLOT-smOVcDxFW-QcC9DFF_JNI130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557115.RA6r3eW66pd9Jyx322yNLOT-smOVcDxFW-QcC9DFF_JNI130_provenance.
- NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557119.RA6ZuDSdvJT1bQQ81SbPvhZTq8i8KxgfCFBxRdKZHEyHw130_provenance.
- NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_assertion description "[Although the phenotype of CDKL5 mutation is similar to Rett syndrome caused by MECP2 mutation, the former is characterized by early-onset seizures and association with West syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557124.RA70rkHyHbb4vzYF3ygGBvlIs9IwERqn2tQzJi_G8Rc0U130_provenance.