Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion description "[Among the 15 sporadic SCA patients, genetic mutations for SCA2, SCA6, SCA17, and SCA31 were identified, indicating that ADCAs should be considered in sporadic cases of ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion evidence source_evidence_literature NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion SIO_000772 21088341 NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion wasDerivedFrom befree-2016 NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion wasGeneratedBy ECO_0000203 NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- befree-2016 importedOn "2016-02-19" NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.