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- NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_assertion type Assertion NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_head.
- NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_assertion wasGeneratedBy ECO_0000203 NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_provenance.
- NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_assertion wasDerivedFrom gad-20150221 NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_provenance.
- NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_assertion SIO_000772 18981294 NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_provenance.
- NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_assertion evidence source_evidence_literature NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_provenance.
- NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_assertion description "[Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132629.RAi9FvElWYEdMyu_MF2r7jNdPkVoizEqLAswwWUSOjRyM130_provenance.