Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_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." NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_assertion evidence source_evidence_literature NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_assertion SIO_000772 14756671 NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_assertion wasDerivedFrom befree-2016 NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_assertion wasGeneratedBy ECO_0000203 NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.
- befree-2016 importedOn "2016-02-19" NP430327.RA7sQjX-UOcMSG71uRG3zhhKX4MY8qAg7AlkfDbcIPkew130_provenance.