Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- befree-2016 importedOn "2016-02-19" NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_assertion wasGeneratedBy ECO_0000203 NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_assertion wasDerivedFrom befree-2016 NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_assertion SIO_000772 20669327 NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_assertion evidence source_evidence_literature NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.
- NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_assertion description "[Mutations in PRKN, DJ-1, and PINK1 are associated with a rather pure parkinsonian phenotype, and have a more benign course with sustained treatment response and absence of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829455.RAAqbUn3aPgia12d0aDwdqID0N3LpxC-j0MNjdL_fxL3o130_provenance.