Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_assertion description "[The two closely linked genes are located on chromosome 6p, between HLA-B and -DR. Several reports have established complete C4B deficiency as the major genetic risk factor for IgA nephropathy (RR = 6.5; p = 0.0004).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_assertion evidence source_evidence_literature NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_assertion SIO_000772 2573592 NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_assertion wasDerivedFrom befree-20140225 NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_assertion wasGeneratedBy ECO_0000203 NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP674536.RAHxQyV_jmltw9jrlU8RiVsvQMfBTDsR7QfVih1IWthFA130_provenance.