Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_assertion description "[We determined the prevalence of SCA2 and SCA3 mutations in a cohort of ET and atypical Parkinsonism patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_assertion evidence source_evidence_literature NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_assertion SIO_000772 17712857 NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_assertion wasDerivedFrom lhgdn-20090331 NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_assertion wasGeneratedBy ECO_0000203 NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP228459.RAjyEF2ELrFOFkYgT1jlcWzdMu9-_h81XoWPTxmdGUBbY130_provenance.