Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_assertion> ?p ?o ?g. }
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- NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_assertion type Assertion NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_head.
- NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_assertion wasGeneratedBy ECO_0000203 NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_provenance.
- NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_assertion wasDerivedFrom lhgdn-20090331 NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_provenance.
- NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_assertion SIO_000772 16358335 NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_provenance.
- NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_assertion evidence source_evidence_literature NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_provenance.
- NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_assertion description "[Two families with SNCA duplication were identified among autosomal dominant hereditary Parkinson's disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193777.RAE4BGsy4ASMiKByEKkeZ7gRUoc4osK-90mfSMMsIb5MQ130_provenance.