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- NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_assertion type Assertion NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_head.
- NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_assertion wasGeneratedBy ECO_0000203 NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_provenance.
- NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_assertion wasDerivedFrom befree-2016 NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_provenance.
- NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_assertion SIO_000772 22236427 NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_provenance.
- NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_assertion evidence source_evidence_literature NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_provenance.
- NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_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." NP952444.RA6nOYd_ab3bFJM3p1pj_AxpVdNvYmxqg-Vgu65jE4VlQ130_provenance.