Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_assertion type Assertion NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_head.
- NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_assertion wasGeneratedBy ECO_0000203 NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_provenance.
- NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_assertion wasDerivedFrom befree-20150227 NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_provenance.
- NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_assertion SIO_000772 21035104 NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_provenance.
- NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_assertion evidence source_evidence_literature NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_provenance.
- NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_assertion description "[Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615154.RAPWqtWDp8h64ZFtBfA4kNarw4STXZPrQSaBU1wDwGK1k130_provenance.