Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_assertion> ?p ?o ?g. }
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- NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_assertion type Assertion NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_head.
- NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_assertion description "[Here, we identified two de novo mutations in patients with sporadic SCZ in GRIN2A and one de novo mutation in GRIN2B in a patient with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_provenance.
- NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_assertion evidence source_evidence_literature NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_provenance.
- NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_assertion SIO_000772 22833210 NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_provenance.
- NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_assertion wasDerivedFrom befree-2016 NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_provenance.
- NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_assertion wasGeneratedBy ECO_0000203 NP1000431.RAvADRPdRLtkhfWssaz7tr6XGKrQv7ckcxfABkRZAKLdM130_provenance.