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- NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_assertion type Assertion NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_head.
- NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_assertion wasGeneratedBy ECO_0000203 NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_provenance.
- NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_assertion wasDerivedFrom gad-20130706 NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_provenance.
- NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_assertion SIO_000772 18981294 NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_provenance.
- NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_assertion evidence source_evidence_literature NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_provenance.
- NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_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." NP78108.RA_FET0jDwpEV91s2zNQpcNTAcCgJly5_rTRSPh8QiS2I130_provenance.