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- source_evidence_literature type ECO_0000212 NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP933101.RAuVLW_3oP3XKc6a3TbKENu0sfKZ01Ma7URErI_OcPKJE130_provenance.