Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_assertion> ?p ?o ?g. }
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- NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_assertion type Assertion NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_head.
- NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_assertion wasGeneratedBy ECO_0000218 NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_provenance.
- NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_assertion wasDerivedFrom uniprot-2016 NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_provenance.
- NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_assertion SIO_000772 20493458 NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_provenance.
- NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_assertion evidence source_evidence_curated NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_provenance.
- NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_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." NP6219.RA-koJKv46m2nJPkuQwtWaCuRKaHUEa8Cy9Y-NjVuwKT0130_provenance.