Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_assertion description "[We identified a homozygous, loss-of-function mutation in PRKCD (PKC?) in a patient who presented with chronic lymphadenopathy, splenomegaly, autoantibodies, elevated immunoglobulins and natural killer dysfunction associated with chronic, low-grade Epstein-Barr virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_assertion evidence source_evidence_literature NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_assertion SIO_000772 23430113 NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_assertion wasDerivedFrom befree-20140225 NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_assertion wasGeneratedBy ECO_0000203 NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP677004.RALTzmmwJtnSrVtOoLxVFfhrZLH2vsRV3wvGt-y0kuYvQ130_provenance.