Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_assertion type Assertion NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_head.
- NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_assertion wasGeneratedBy ECO_0000203 NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_provenance.
- NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_assertion wasDerivedFrom befree-20140225 NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_provenance.
- NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_assertion SIO_000772 11496370 NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_provenance.
- NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_assertion evidence source_evidence_literature NP580093.RAfUZAhsC8wIXUbSs7ZZOxZZf38mvfS0fT2HnaCtzI3F4130_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.