Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_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." NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_assertion evidence source_evidence_literature NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_assertion SIO_000772 20004785 NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_assertion wasDerivedFrom befree-2016 NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_assertion wasGeneratedBy ECO_0000203 NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.
- befree-2016 importedOn "2016-02-19" NP780862.RANlmB-DlR8lzJuMzTgreAEpuSms5q1owADqbA-SLeKc0130_provenance.