Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_assertion> ?p ?o ?g. }
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- NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_assertion type Assertion NP563292.RAbHV4HSFrHOvhrSQpjzXOEGqgVchZ6bdAOXKgY9DsEbs130_head.
- 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.