Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_assertion> ?p ?o ?g. }
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- NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_assertion type Assertion NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_head.
- NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_assertion wasGeneratedBy ECO_0000203 NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_provenance.
- NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_assertion wasDerivedFrom befree-20150227 NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_provenance.
- NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_assertion SIO_000772 18981294 NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_provenance.
- NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_assertion evidence source_evidence_literature NP873884.RADhKxz5wpRcr-edI2dz-yQSI55EDy450BKA2Baud_dcE130_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.