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- NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_assertion type Assertion NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_head.
- NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_assertion description "[Recently mutations in the SLC16A2 gene coding for the monocarboxylate thyroid hormone transporter 8, MCT8, have been associated with Allan-Herndon-Dudley syndrome (AHDS), an X-linked condition characterized by severe mental retardation, dysarthria, athetoid movements, muscle hypoplasia and spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_provenance.
- NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_assertion evidence source_evidence_literature NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_provenance.
- NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_assertion SIO_000772 20713192 NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_provenance.
- NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_assertion wasDerivedFrom befree-2016 NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_provenance.
- NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_assertion wasGeneratedBy ECO_0000203 NP833022.RAdLKLRMShu1bg55PgVf--l9FoIaV6EfEYv_ev6i-9H-w130_provenance.