Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_assertion description "[The AS isoform lacks exon 8, and is deduced to contain 49 amino acid changes in the membrane-distal portion of the extracellular domain, where considerable amino acid changes are known in CD72(c) allele associated with murine SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_assertion evidence source_evidence_literature NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_assertion SIO_000772 15459183 NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_assertion wasDerivedFrom befree-20140225 NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_assertion wasGeneratedBy ECO_0000203 NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP310476.RAvQgHRCr-k86yoc6mUKOlSdkUrU09kp6KxkOpsjptLvs130_provenance.