Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_assertion> ?p ?o ?g. }
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- NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_assertion type Assertion NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_head.
- NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_assertion description "[Spinocerebellar ataxia 2 (SCA2) is an autosomal dominant neurodegenerative disorder that results from the expansion of a cryptic CAG repeat within the exon 1 of the SCA2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_provenance.
- NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_assertion evidence source_evidence_literature NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_provenance.
- NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_assertion SIO_000772 11689490 NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_provenance.
- NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_assertion wasDerivedFrom befree-20140225 NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_provenance.
- NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_assertion wasGeneratedBy ECO_0000203 NP368861.RAwZlfhxp7JYrjj1X5Cz0-hYtwXTegGxI0R_uXmnMedA0130_provenance.