Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_assertion> ?p ?o ?g. }
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- NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_assertion type Assertion NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_head.
- NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_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." NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_provenance.
- NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_assertion evidence source_evidence_literature NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_provenance.
- NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_assertion SIO_000772 22833210 NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_provenance.
- NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_assertion wasDerivedFrom befree-20150227 NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_provenance.
- NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_assertion wasGeneratedBy ECO_0000203 NP434624.RAUZ98j0vCNfTYUi6dLSe9lLTETe2ElYlNUDehJUqDHfo130_provenance.