Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_assertion description "[The aim of the study was: 1) to evaluate the prevalence of the DYT1 mutation in a population of Polish patients with early-onset generalized dystonia and with other forms of familial dystonia, 2) to evaluate the frequency of the DYT1 mutation in patients with writer's cramp, 3) to characterize the phenotype of the DYT1 mutation in the Polish population, and 4) to define the group of patients in whom genetic testing is recommended.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_assertion evidence source_evidence_literature NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_assertion SIO_000772 18224570 NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_assertion wasDerivedFrom befree-2016 NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_assertion wasGeneratedBy ECO_0000203 NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.
- befree-2016 importedOn "2016-02-19" NP652113.RAfTxPDV7A7IhZDxGOyLXgZ-e_vYea2fFfpf9jp0Pgnlg130_provenance.