Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- befree-2016 importedOn "2016-02-19" NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_assertion wasGeneratedBy ECO_0000203 NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_assertion wasDerivedFrom befree-2016 NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_assertion SIO_000772 12584415 NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_assertion evidence source_evidence_literature NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.
- NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_assertion description "[Various deletions and point mutations in the Parkin gene have been strongly associated with Parkinson's disease (PD) and parkinsonism, especially when the onset occurs at a young age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383714.RACcU-EOtUv2-pd-tL2qq4owIfMh7BK3_-ym97Zh6UmcA130_provenance.