Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_assertion> ?p ?o ?g. }
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- NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_assertion type Assertion NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_head.
- NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_assertion wasGeneratedBy ECO_0000203 NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_provenance.
- NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_assertion wasDerivedFrom befree-2016 NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_provenance.
- NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_assertion SIO_000772 22236427 NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_provenance.
- NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_assertion evidence source_evidence_literature NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_provenance.
- NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_assertion description "[The discovery that loss-of-function mutations in the gene DOCK8 are responsible for most forms of autosomal recessive hyper-IgE syndrome and some forms of combined immunodeficiency without elevated serum IgE has led to studies into the immunopathogenesis of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952445.RABgj4hAOTA1W96rKph6dGB9Z1wW3OaIgrzuBiifkJ82I130_provenance.