Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_assertion description "[This contrasts with homozygous parkin, PINK1 or DJ1 parkinsonism, characterized by young-onset (usually <40 years), and a comparatively benign course of predominantly levodopa-responsive symptoms without dementia or prominent dysautonomia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_assertion evidence source_evidence_literature NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_assertion SIO_000772 19815446 NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_assertion wasDerivedFrom befree-20150227 NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_assertion wasGeneratedBy ECO_0000203 NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP940544.RAGVxh741Ey7y0jlQyuKd6r4gvf_7MuW-RbL0nhJ9HSFY130_provenance.