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- NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_assertion type Assertion NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_head.
- NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_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." NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.
- NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_assertion evidence source_evidence_literature NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.
- NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_assertion SIO_000772 22019273 NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.
- NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_assertion wasDerivedFrom befree-20150227 NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.
- NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_assertion wasGeneratedBy ECO_0000203 NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.