Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_assertion description "[Because sTNFRIIs can act as TNF antagonists, the association between recipient and donor TNFRII 196R allele status and acute or extensive chronic GVHD incidence, respectively, may reflect reduced circulating sTNFRII.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_assertion evidence source_evidence_literature NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_assertion SIO_000772 14688526 NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_assertion wasDerivedFrom gad-20150221 NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_assertion wasGeneratedBy ECO_0000203 NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP151408.RApdjifs3V9TfSEbTZ3ScgL35n9r-i9d7X5jSj_ViMCgE130_provenance.