Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_assertion description "[DOCK8 disruption is associated with a phenotype of severe cellular immunodeficiency characterized by susceptibility to viral infections, atopic eczema, defective T-cell activation and T(h)17 cell differentiation, and impaired eosinophil homeostasis and dysregulation of IgE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_assertion evidence source_evidence_literature NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_assertion SIO_000772 20004785 NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_assertion wasDerivedFrom befree-2016 NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_assertion wasGeneratedBy ECO_0000203 NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP780860.RAhB0Nr5hqBdqenoYSMDwTaByGnSNQ3aRexh0YQULkAr4130_provenance.