Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_assertion description "[Mutations in the ACTN4 gene cause focal segmental glomerulosclerosis (FSGS), which shows autosomal dominant inheritance (Online Mendelian Inheritance in Man No.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_assertion evidence source_evidence_literature NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_assertion SIO_000772 18436095 NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_assertion wasDerivedFrom befree-20140225 NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_assertion wasGeneratedBy ECO_0000203 NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP448646.RAfVt3_H7Pnf4gflkSzU8nVm9G1pPKqveyWHLMDUG7lmg130_provenance.