Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- 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.
- NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_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." NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_provenance.
- NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_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." NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_provenance.
- NP701447.RAUNzh9-z5DP-mWm7PtaX7LHexL4b0tCZrsiA9aIcJiYU130_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." NP701447.RAUNzh9-z5DP-mWm7PtaX7LHexL4b0tCZrsiA9aIcJiYU130_provenance.
- 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." provenance.
- 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." 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.