Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_assertion wasGeneratedBy ECO_0000203 NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_assertion wasDerivedFrom befree-2016 NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_assertion SIO_000772 22865047 NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_assertion evidence source_evidence_literature NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.
- NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_assertion description "[Nonetheless, CNVs in FCGR3B, DEFB4, CCL3L1, C4A/B and NCF1 have been suggested to be associated with autoimmune diseases, although there is conflicting evidence in all cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002932.RA3dfvA4v7s4Fzl1dY4VwzMFXb8sPgouFapHR3o5t4yiA130_provenance.