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- NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_assertion type Assertion NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_head.
- NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_assertion description "[Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.
- NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_assertion evidence source_evidence_literature NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.
- NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_assertion SIO_000772 22019273 NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.
- NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_assertion wasDerivedFrom befree-20150227 NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.
- NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_assertion wasGeneratedBy ECO_0000203 NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.