Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_assertion description "[The incidence of GVHD in matched and unmatched groups was respectively: grade I-IV: 81% and 86% (P = 0.492); II-IV 61% and 57% (P = 0.495); III-IV 23% and 21% (P = 0.608).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_assertion evidence source_evidence_literature NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_assertion SIO_000772 17130788 NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_assertion wasDerivedFrom befree-2016 NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_assertion wasGeneratedBy ECO_0000203 NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.
- befree-2016 importedOn "2016-02-19" NP581340.RASpZlUPReHojVwFbftSwW4AJcMkks4fveej07iUlVzDk130_provenance.