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- NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_assertion type Assertion NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_head.
- NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_assertion wasGeneratedBy ECO_0000203 NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_provenance.
- NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_assertion wasDerivedFrom befree-20150227 NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_provenance.
- NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_assertion SIO_000772 10844531 NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_provenance.
- NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_assertion evidence source_evidence_literature NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_provenance.
- NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_assertion description "[To examine the possibility that sporadic male cases with X-linked agammaglobulinaemia (XLA), which is caused by mutations in the Bruton's tyrosine kinase (Btk) gene, might be misregistered as having CVID, we employed a flow cytometric test to identify XLA in hypogammaglobulinaemic males registered as CVID in the Japanese Immunodeficiency Registry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274759.RABKYPkicImshVhsdgX5TN_pxzJROZ4tUWryjhRIs4dWM130_provenance.