Matches in Nanopublications for { ?s ?p "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905282.RAh52luulgnzv5dpHn78-ms5lJCP5TWMLrBW6UyZVTjqI130_provenance.
- NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
- NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439494.RAMR084aMUA9FmdfeEGzwbT1PL2eumQtoLXmU8voGiE-0130_provenance.
- assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733184.RAPZH01xLgRi2wMCxYtZDUIhGHwbIBYEcjgKUmppO1NeA130_provenance.
- NP434668.RAq9WaoCH3MFUTo6XNdw6WaQ541AYgBP6Hxj9g0-M4ovs130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434668.RAq9WaoCH3MFUTo6XNdw6WaQ541AYgBP6Hxj9g0-M4ovs130_provenance.
- NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_provenance.
- NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1000432.RA5AqQZpq9aeI2_rEZTO9T9O3fouoNSfsN4aPYLb-hmXo130_provenance.
- NP1000434.RA3Jgpxa9oBfOcWkUxu_Ckqyy7oj57s8txNURQeOkfKsc130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1000434.RA3Jgpxa9oBfOcWkUxu_Ckqyy7oj57s8txNURQeOkfKsc130_provenance.