Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_assertion type Assertion NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_head.
- NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_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." NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_provenance.
- NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_assertion evidence source_evidence_literature NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_provenance.
- NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_assertion SIO_000772 22833210 NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_provenance.
- NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_assertion wasDerivedFrom befree-20150227 NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_provenance.
- NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_assertion wasGeneratedBy ECO_0000203 NP434588.RAaTBL9FugLIRcz_M4ZqcrtE7-8dZ95YViOpGE3n8ymSc130_provenance.