Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_assertion description "[Suppressor of cytokine signalling (SOCS)1 and SOCS3 epigenetic silencing were occasionally detected, whereas SOCS1 was frequently mutated in diffuse large B-cell lymphoma and polymorphic post-transplant lymphoproliferative disorders, possibly as a cause of aberrant somatic hypermutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_assertion evidence source_evidence_literature NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_assertion SIO_000772 22488585 NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_assertion wasDerivedFrom befree-20140225 NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_assertion wasGeneratedBy ECO_0000203 NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP694463.RAsLq10q5qPABWzAUBoU7cxJHj57cInOCkb1LIXnk5ZMo130_provenance.