Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_assertion wasGeneratedBy ECO_0000203 NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_assertion wasDerivedFrom befree-20150227 NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_assertion SIO_000772 17440947 NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_assertion evidence source_evidence_literature NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.
- NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_assertion description "[Recent reports suggest that CAG triplet expansions of spinocerebellar ataxia type 2 and 3 (SCA2 and SCA3) genes are the cause of typical levodopa-responsive Parkinson's disease (PD) in familial cases, several of which were ethnic Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557489.RAesmmR_CDo-fXyNpFXYM36j6L1-a5mnZRMCPzmYYW2iA130_provenance.