Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_assertion> ?p ?o ?g. }
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- NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_assertion type Assertion NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_head.
- NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_assertion description "[Currently 14 registries are distributed, including information about Bloom syndrome (BLMbase), X-linked agammaglobulinemia (BTKbase), X-linked and autosomal recessive chronic granulomatous diseases (CYBBbase for X-linked CGD, CYBAbase for p22(phox) deficiency, NCF1base for p47(phox) deficiency, NCF2base for p67(phox) deficiency), CD3gamma and CD3epsilon deficiencies (CD3Gbase, CD3Ebase), X-linked hyper-IgM syndrome (CD40Lbase), T-B+ severe combined immunodeficiency (JAK3base), V(D)J recombination defects (RAG1base, RAG2base), X-linked lymphoproliferative syndrome (SH2D1Abase), and ZAP-70 deficiency (ZAP70base).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_provenance.
- NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_assertion evidence source_evidence_literature NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_provenance.
- NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_assertion SIO_000772 11213802 NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_provenance.
- NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_assertion wasDerivedFrom befree-2016 NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_provenance.
- NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_assertion wasGeneratedBy ECO_0000203 NP308864.RACeVmoNm14Vp85YuXXCBte0-MiLNoww_FIsSFtIg0sTk130_provenance.