Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_assertion description "[The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_assertion evidence source_evidence_literature NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_assertion SIO_000772 17282997 NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_assertion wasDerivedFrom befree-2016 NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_assertion wasGeneratedBy ECO_0000203 NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.
- befree-2016 importedOn "2016-02-19" NP592424.RAXPSA0YRa4nHQNV7L_Svk-xsltoIFZbw-kOWDRuwt-Io130_provenance.