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- NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_assertion type Assertion NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_head.
- NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_assertion description "[Carbohydrate-deficient glycoprotein syndrome type 1 (CDG1) (MIM: 212065) is an autosomal recessive disorder with psychomotor retardation, strokelike episodes, ataxia, and olivopontocerebellar atrophy (OPCA) of neonatal onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_provenance.
- NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_assertion evidence source_evidence_literature NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_provenance.
- NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_assertion SIO_000772 10066032 NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_provenance.
- NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_assertion wasDerivedFrom befree-20150227 NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_provenance.
- NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_assertion wasGeneratedBy ECO_0000203 NP632228.RAlZg543fvGfAostjEiGotD_AvbDHtjOKv6nw3SWytVEM130_provenance.