Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_assertion description "[Loss-of-function mutations in PARK2, the gene encoding the E3 ubiquitin ligase Parkin, are the most frequent cause of recessive Parkinson's disease (PD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_assertion evidence source_evidence_literature NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_assertion SIO_000772 24852371 NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_assertion wasDerivedFrom befree-2016 NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_assertion wasGeneratedBy ECO_0000203 NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1184598.RAT4d9nH-2VZZcKFp4IP05Lgvx9IFdAzBOXtPqglFWrYU130_provenance.