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Matches in Nanopublications for { ?s ?p "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP210018.RAdpzvvI6esYZixQvImx5gJSaBpwDsRpswPQoe3ytUELQ130_assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210018.RAdpzvvI6esYZixQvImx5gJSaBpwDsRpswPQoe3ytUELQ130_provenance.
• NP404877.RAoP1DAnHTbKQygr7SXQDW5eXlul-GOaePn-whmtb6adk130_assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404877.RAoP1DAnHTbKQygr7SXQDW5eXlul-GOaePn-whmtb6adk130_provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP983482.RAfHuvrLF37SELVLUX-hWL8Hmeg4rzDhwqCsDvPF4rJvI130_assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983482.RAfHuvrLF37SELVLUX-hWL8Hmeg4rzDhwqCsDvPF4rJvI130_provenance.
• NP826628.RACKm3j_Z0ypSiwGZyHGqKr3jqo5rH2AGwAh3bJ0EVhts130_assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826628.RACKm3j_Z0ypSiwGZyHGqKr3jqo5rH2AGwAh3bJ0EVhts130_provenance.
• NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.