Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_assertion description "[abnormal expansions of an allele in SCA8 and SCA17 genes were detected in patients with both Parkinson's disease and spinocerebellar ataxia]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_assertion evidence source_evidence_literature NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_assertion SIO_000772 14756671 NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_assertion wasDerivedFrom lhgdn-20090331 NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_assertion wasGeneratedBy ECO_0000203 NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193684.RAJQW9UG5fjL8VgFd1ed5Ew7Su16OA_X9v3LG7haGWWbw130_provenance.