Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_assertion> ?p ?o ?g. }
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- NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_assertion type Assertion NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_head.
- NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_assertion wasGeneratedBy ECO_0000218 NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_provenance.
- NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_assertion wasDerivedFrom ctd_human-2016 NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_provenance.
- NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_assertion SIO_000772 20493458 NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_provenance.
- NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_assertion evidence source_evidence_curated NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_provenance.
- NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_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." NP26212.RA2-IZsVSlA9hzouwZ3PfuM6viHbKozQiEU-Z_3friTU8130_provenance.