Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_assertion> ?p ?o ?g. }
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- NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_assertion type Assertion NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_head.
- NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_assertion wasGeneratedBy ECO_0000203 NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_provenance.
- NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_assertion wasDerivedFrom befree-2016 NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_provenance.
- NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_assertion SIO_000772 21035104 NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_provenance.
- NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_assertion evidence source_evidence_literature NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_provenance.
- NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_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." NP849097.RAAVyuUMXVXF8OHfnn5CpAKFW0JOP1gAIqNpnPuufOn6k130_provenance.