Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP26209.RAWxR7th1wzLiW6DQSGtUALPCPaN3nUaYv0FNgw9AVYU4130_provenance.
- 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.