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- NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_assertion type Assertion NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_head.
- NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_assertion wasGeneratedBy ECO_0000203 NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_provenance.
- NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_assertion wasDerivedFrom befree-20140225 NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_provenance.
- NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_assertion SIO_000772 13129599 NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_provenance.
- NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_assertion evidence source_evidence_literature NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_provenance.
- NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_assertion description "[Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266251.RA45it8-JhdP4pJsET5J9oy6V9FEjiDrvQFKuM_4TryfM130_provenance.