Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_assertion type Assertion NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_head.
- NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_assertion wasGeneratedBy ECO_0000218 NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_provenance.
- NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_assertion wasDerivedFrom ctd_human-20150221 NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_provenance.
- NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_assertion SIO_000772 20493458 NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_provenance.
- NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_assertion evidence source_evidence_curated NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_provenance.
- NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_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." NP18453.RAmOiM1Yx7Txs_FbrrPeOwPRSmGVCsWfgs9RUYZktdhe4130_provenance.