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- NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_assertion type Assertion NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_head.
- NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_assertion description "[Blau syndrome is a hereditary granulomatous disease caused by mutations in the CARD15 gene that is diagnosed in children of young age with exanthema/erythema, arthritis/periarthritis and/or uveitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_provenance.
- NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_assertion evidence source_evidence_literature NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_provenance.
- NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_assertion SIO_000772 17207093 NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_provenance.
- NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_assertion wasDerivedFrom befree-2016 NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_provenance.
- NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_assertion wasGeneratedBy ECO_0000203 NP587514.RAANeR1hADuCbFXpdL7hzxt4it3-m2l0_kdIu4EYbOpMU130_provenance.