Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_assertion description "[Aside from the underlying mutations that cause haemophilia A, inhibitor risk appears to be modified by polymorphisms in various cytokines and immunomodulators including IL10, TNF? and CTLA4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_assertion evidence source_evidence_literature NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_assertion SIO_000772 21362111 NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_assertion wasDerivedFrom befree-20140225 NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_assertion wasGeneratedBy ECO_0000203 NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP467761.RAGM1NcVspeNGVgrttifxSPDHlmrGmcyZPTEW29qQv_4U130_provenance.