Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_assertion description "[B2M-deficient cases encompassed most of the nodular sclerosis subtype cases and only a minority of mixed cellularity cases, suggesting that B2M deficiency determines the tumor microenvironment and may define a major subset of cHL that has more uniform clinical and morphologic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_assertion evidence source_evidence_literature NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_assertion SIO_000772 25488972 NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_assertion wasDerivedFrom befree-2016 NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_assertion wasGeneratedBy ECO_0000203 NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246329.RAnK1lAFs5C4401x-Decsq6DPDRZ-1e36Q-lJ8AVUg2bI130_provenance.