Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_assertion> ?p ?o ?g. }
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- NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_assertion type Assertion NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_head.
- NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_assertion wasGeneratedBy ECO_0000203 NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_provenance.
- NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_assertion wasDerivedFrom lhgdn-20090331 NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_provenance.
- NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_assertion SIO_000772 16358335 NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_provenance.
- NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_assertion evidence source_evidence_literature NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_provenance.
- NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_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." NP193797.RAcJx7tgG5lTBcrZs9y4mEZgRAmdVHz74bosUV49V_Co0130_provenance.