Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP262853.RAaw45GnPJj-zaQcieUtWQ_T4rnYHwxB3h-og2-S4CsQ4130_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." NP262853.RAaw45GnPJj-zaQcieUtWQ_T4rnYHwxB3h-og2-S4CsQ4130_provenance.
- NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_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." NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_provenance.
- NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_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." NP554546.RAxXSWMnWnT_6uuS-nngLLgU9g3_CCGhszwoH6_AkkqH8130_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.
- NP326687.RAzA2QW-yipGWeXsG5Q665wlEk8nuUSBiQxq4r5_bnlwI130_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." NP326687.RAzA2QW-yipGWeXsG5Q665wlEk8nuUSBiQxq4r5_bnlwI130_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.
- NP765894.RAEsbRssZZKAuZN66zlUjbOaId8hYOllbxlhSJvQk2p_8130_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." NP765894.RAEsbRssZZKAuZN66zlUjbOaId8hYOllbxlhSJvQk2p_8130_provenance.