Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_assertion description "[No association was observed for TNFR2, FCGR, or CTLA4 with MPA, nor with the presence of MPO-ANCA, although the combined genotype FCGR2A-131H/H and 3A-176F/F was increased in patients with MPA (p = 0.025).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_assertion evidence source_evidence_literature NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_assertion SIO_000772 12858454 NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_assertion wasDerivedFrom befree-20150227 NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_assertion wasGeneratedBy ECO_0000203 NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP335714.RA1QSnOGRs89vNrUrEDSrpOl4tl7Mi9EMInZFKlewSkwM130_provenance.