Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_assertion> ?p ?o ?g. }
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- NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_assertion type Assertion NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_head.
- NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_assertion wasGeneratedBy ECO_0000218 NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_provenance.
- NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_assertion wasDerivedFrom ctd_human-20150221 NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_provenance.
- NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_assertion SIO_000772 20493458 NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_provenance.
- NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_assertion evidence source_evidence_curated NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_provenance.
- NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_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." NP18455.RA-4FEqIRfAHcA-Ad_VNAauhh0-sleCoa0aZ8fP8uymqo130_provenance.