Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_assertion description "[Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_assertion evidence source_evidence_literature NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_assertion SIO_000772 19205068 NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_assertion wasDerivedFrom befree-20140225 NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_assertion wasGeneratedBy ECO_0000203 NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP165214.RAyz8zQzgmhCxdwF2v9To030dxKUzJjG9_q-bgkbMLYJ4130_provenance.