Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_assertion> ?p ?o ?g. }
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- NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_assertion type Assertion NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_head.
- NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_assertion wasGeneratedBy ECO_0000203 NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_provenance.
- NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_assertion wasDerivedFrom gad-20150221 NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_provenance.
- NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_assertion SIO_000772 15679701 NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_provenance.
- NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_assertion evidence source_evidence_literature NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_provenance.
- NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_assertion description "[Our study supports the notion that primary dystonia is a genetically heterogeneous disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90338.RARiM9O6jcYDfi-kk3JpSYMt_MLbfXtV91kFCGdf4z3Ko130_provenance.