Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_assertion description "[Interindividual gene copy-number variation (CNV) of complement component C4 and its associated polymorphisms in gene size (long and short) and protein isotypes (C4A and C4B) probably lead to different susceptibilities to autoimmune disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_assertion evidence source_evidence_literature NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_assertion SIO_000772 17503323 NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_assertion wasDerivedFrom befree-20140225 NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_assertion wasGeneratedBy ECO_0000203 NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP856106.RAI4G3NN5SgxieGNcc3nXmRH6PKiOMy2qMs9QwiIlHD3g130_provenance.