Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_assertion description "[XMEN disease (X-linked immunodeficiency with Magnesium defect, Epstein-Barr virus infection and Neoplasia) is a novel primary immune deficiency caused by mutations in MAGT1 and characterised by chronic infection with Epstein-Barr virus (EBV), EBV-driven lymphoma, CD4 T-cell lymphopenia, and dysgammaglobulinemia [1].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_assertion evidence source_evidence_literature NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_assertion SIO_000772 25504528 NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_assertion wasDerivedFrom befree-2016 NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_assertion wasGeneratedBy ECO_0000203 NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248048.RAtcs0JDx3mWPTvwaLrisPX7Sbr7AV9QKkcJSA7xoQtBg130_provenance.