Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_assertion description "[No significant differences in allele (T allele frequency: 49.7% in patients with pSS versus 50% in controls; P = 0.94) and genotype frequencies of BAFF polymorphism were detected between pSS patients and control individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_assertion evidence source_evidence_literature NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_assertion SIO_000772 16507129 NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_assertion wasDerivedFrom befree-2016 NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_assertion wasGeneratedBy ECO_0000203 NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.
- befree-2016 importedOn "2016-02-19" NP537956.RA4UEpydz7QuEpb7LsBHhs0S5GqcY5fubjICC7MvHd_uY130_provenance.