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- NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_assertion type Assertion NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_head.
- NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_assertion description "[Type 1 hyper-IgM syndrome (HIGM1) is a rare primary immunodeficiency disease caused by mutations in the CD40L gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_provenance.
- NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_assertion evidence source_evidence_literature NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_provenance.
- NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_assertion SIO_000772 24768948 NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_provenance.
- NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_assertion wasDerivedFrom befree-20150227 NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_provenance.
- NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_assertion wasGeneratedBy ECO_0000203 NP295376.RAqOPQaUmPP_I3ifwM5EQS_-_hcRCXbgLU1lVYYh693U4130_provenance.