Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion type Assertion NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_head.
- NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_provenance.
- NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion evidence source_evidence_literature NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_provenance.
- NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion SIO_000772 19034539 NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_provenance.
- NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion wasDerivedFrom befree-2016 NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_provenance.
- NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_assertion wasGeneratedBy ECO_0000203 NP705780.RAeg0OfAlZa4sZy2CY59jbK2geJ0NdaS7G1tO1CqHY2OE130_provenance.