Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_assertion description "[The relative risk of LL patients with the C4B*Q0 allele suffering from ENL was 5.3 compared with LL patients without C4B*Q0.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_assertion evidence source_evidence_literature NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_assertion SIO_000772 8485914 NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_assertion wasDerivedFrom befree-20140225 NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_assertion wasGeneratedBy ECO_0000203 NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP446579.RARRmuSR1_ZMhxTIGziqsLJq7u1VVby9MP_sxbrM4t7MY130_provenance.