Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_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." NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_assertion evidence source_evidence_literature NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_assertion SIO_000772 16507129 NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_assertion wasDerivedFrom befree-20150227 NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_assertion wasGeneratedBy ECO_0000203 NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP851308.RAfMl-NGvGoqejuhkRuzSQ17rAfNSuTFvf0uqVUQmBLy0130_provenance.