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- NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_assertion type Assertion NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_head.
- NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_assertion description "[Segawa disease (autosomal dominant guanosine triphosphate cyclohydrolase I [GTP-I] deficiency, DYT5) is a hereditary dopa-responsive generalized dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_provenance.
- NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_assertion evidence source_evidence_literature NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_provenance.
- NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_assertion SIO_000772 17389309 NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_provenance.
- NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_assertion wasDerivedFrom befree-2016 NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_provenance.
- NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_assertion wasGeneratedBy ECO_0000203 NP601215.RABZN8dC1uKxmPpKP5U__RqUlMO-zoH1JhE2gvvunezTM130_provenance.