Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_assertion description "[These findings suggested that the functional SNP BLK rs2248932 T/C variant allele was associated with RA development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_assertion evidence source_evidence_literature NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_assertion SIO_000772 22740142 NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_assertion wasDerivedFrom befree-20140225 NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_assertion wasGeneratedBy ECO_0000203 NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_provenance.