Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_assertion> ?p ?o ?g. }
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- NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_assertion type Assertion NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_head.
- NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_assertion wasGeneratedBy ECO_0000218 NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_assertion wasDerivedFrom ctd_human-2016 NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_assertion SIO_000772 20493458 NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_assertion evidence source_evidence_curated NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_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." NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.