Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_assertion> ?p ?o ?g. }
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- NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_assertion type Assertion NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_head.
- 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.
- NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_assertion evidence source_evidence_literature NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_provenance.
- NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_assertion SIO_000772 22833210 NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_provenance.
- NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_assertion wasDerivedFrom befree-20150227 NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_provenance.
- NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_assertion wasGeneratedBy ECO_0000203 NP434561.RAHLKvITM0FSGM0pxs5J6-4PNjhwzQFoNVcE4SSkyM_l4130_provenance.