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- NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_assertion type Assertion NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_head.
- NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_assertion wasGeneratedBy ECO_0000203 NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_provenance.
- NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_assertion wasDerivedFrom befree-2016 NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_provenance.
- NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_assertion SIO_000772 19641205 NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_provenance.
- NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_assertion evidence source_evidence_literature NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_provenance.
- NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_assertion description "[We describe AGC1 deficiency, a novel syndrome characterized by arrested psychomotor development, hypotonia, and seizures in a child with a homozygous missense mutation in the solute carrier family 25, member 12, gene SLC25A12, which encodes the AGC1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754276.RAAi4sE5p6d7yYrYCbumOdRDi_lqA4_vDRxOW8fz61zKU130_provenance.