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- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion type Assertion NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_head.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion wasGeneratedBy ECO_0000203 NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion wasDerivedFrom befree-20140225 NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion SIO_000772 18981294 NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_assertion evidence source_evidence_literature NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.
- NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_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." NP731656.RAVt-lCEo-om8fgNTeyIhmHDZdq8zHgz07H0Ps4p2JGTg130_provenance.