Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_assertion> ?p ?o ?g. }
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- NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_assertion type Assertion NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_head.
- NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_assertion wasGeneratedBy ECO_0000203 NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_provenance.
- NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_assertion wasDerivedFrom befree-20150227 NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_provenance.
- NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_assertion SIO_000772 11496370 NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_provenance.
- NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_assertion evidence source_evidence_literature NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_provenance.
- NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_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." NP765882.RAUka8i4j85MebVRr_zejh9ehNQ-6x6oHAAXGnLIV3clE130_provenance.