Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_assertion description "[We also analysed 190 patients with multiple-system atrophy with cerebellar features (MSA-C), a phenocopy of SCA23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_assertion evidence source_evidence_literature NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_assertion SIO_000772 23108490 NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_assertion wasDerivedFrom befree-20140225 NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_assertion wasGeneratedBy ECO_0000203 NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP858297.RAfNltHaADFuntg7x9DBXV4LHxf1SN4Nw8QOCTtlBC5K8130_provenance.