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- source_evidence_literature type ECO_0000212 NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP933077.RAXfQzsppY7__qjansQj3tBrJIxh-4nAvphcxk6Divyrw130_provenance.