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- NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_assertion type Assertion NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_head.
- NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_assertion wasGeneratedBy ECO_0000203 NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_provenance.
- NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_assertion wasDerivedFrom befree-20150227 NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_provenance.
- NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_assertion SIO_000772 18981294 NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_provenance.
- NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_assertion evidence source_evidence_literature NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_provenance.
- NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_assertion description "[The genetic complexity and variable clinical presentation of TACI deficiency prompted us to evaluate the genetic, immunologic, and clinical condition in 50 individuals with TNFRSF13B alterations, following screening of 564 unrelated patients with hypogammaglobulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873932.RAkXa7ji-GIORB7mnSump8gMVi07jSEUX5OGprVaQ4dr0130_provenance.