Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_assertion> ?p ?o ?g. }
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- NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_assertion type Assertion NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_head.
- NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_assertion wasGeneratedBy ECO_0000218 NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_provenance.
- NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_assertion wasDerivedFrom ctd_human-20150221 NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_provenance.
- NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_assertion SIO_000772 20493458 NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_provenance.
- NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_assertion evidence source_evidence_curated NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_provenance.
- NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_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." NP18451.RA2VtwdUlZM8dJCDIp6drrw50L-87n5-Q2sRyG5hH_iG0130_provenance.