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- NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_assertion type Assertion NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_head.
- NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_assertion wasGeneratedBy ECO_0000203 NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_provenance.
- NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_assertion wasDerivedFrom befree-2016 NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_provenance.
- NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_assertion SIO_000772 15358621 NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_provenance.
- NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_assertion evidence source_evidence_literature NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_provenance.
- NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_assertion description "[None of the remaining 33 patients (24 males/9 females) had mutations affecting CD40, ICOS, ICOSL, or SH2D1, and are best classified as common variable immune deficiency (CVID), although other genes, including some not yet identified, may be responsible.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459282.RAInb-ClE8CNQSEUYLTQE9NJo9JSNztidqG1v2wfKToTE130_provenance.