Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_assertion> ?p ?o ?g. }
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- NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_assertion type Assertion NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_head.
- NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_assertion wasGeneratedBy ECO_0000203 NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_provenance.
- NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_assertion wasDerivedFrom gad-20150221 NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_provenance.
- NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_assertion SIO_000772 18981294 NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_provenance.
- NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_assertion evidence source_evidence_literature NP115734.RAIPLVUJRircLbLwKtC_U3IyfWBiiG-du_BWuOKq-0AEo130_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.