Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_assertion description "[Parkinson protein 2, E3 ubiquitin protein ligase (PARK2) gene mutations are the most frequent causes of autosomal recessive early onset Parkinson's disease and juvenile Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_assertion evidence source_evidence_literature NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_assertion SIO_000772 25136611 NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_assertion wasDerivedFrom befree-2016 NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_assertion wasGeneratedBy ECO_0000203 NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1211884.RAGG-48bJvFc8Ms1HI9Ru46eYA7xZ1M9gxBMY4MiC6IQs130_provenance.