Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_assertion description "[TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_assertion evidence source_evidence_literature NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_assertion SIO_000772 22980509 NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_assertion wasDerivedFrom befree-2016 NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_assertion wasGeneratedBy ECO_0000203 NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.
- befree-2016 importedOn "2016-02-19" NP1013002.RAFLwLHFTElBp4B8wcY_0rwWNtGhw6gRqF6-yX3C4mqic130_provenance.