Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_assertion description "[Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_assertion evidence source_evidence_literature NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_assertion SIO_000772 14756671 NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_assertion wasDerivedFrom befree-2016 NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_assertion wasGeneratedBy ECO_0000203 NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.
- befree-2016 importedOn "2016-02-19" NP430326.RA-ym3d067wLPBmWyVLbrIjOw8Dawib_Tw71DWIp9EcnA130_provenance.