Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion> ?p ?o ?g. }
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- NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion type Assertion NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_head.
- NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion wasGeneratedBy ECO_0000218 NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_provenance.
- NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion wasDerivedFrom ctd_human-2016 NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_provenance.
- NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion SIO_000772 20493458 NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_provenance.
- NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion evidence source_evidence_curated NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_provenance.
- NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_assertion description "[Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26208.RAf30b3X9kNk2yGLHXtx7eDGSb_0FYAOY4N37KFRNvLNI130_provenance.