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- NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_assertion type Assertion NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_head.
- NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_assertion wasGeneratedBy ECO_0000203 NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_provenance.
- NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_assertion wasDerivedFrom befree-2016 NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_provenance.
- NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_assertion SIO_000772 11496370 NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_provenance.
- NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_assertion evidence source_evidence_literature NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_provenance.
- NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_assertion description "[The results are supportive of UFD1L involvement in the neurodevelopmental origin of schizophrenia and contribute in delineating etiological and pathogenetic mechanism of the schizophrenia subtype related to 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP326680.RAbh3jT7n9yLYfe8h9512GZ4OsJK6qbR-bmJwZcDEbg2s130_provenance.