Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- befree-2016 importedOn "2016-02-19" NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_assertion wasGeneratedBy ECO_0000203 NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_assertion wasDerivedFrom befree-2016 NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_assertion SIO_000772 20023659 NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_assertion evidence source_evidence_literature NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.
- NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_assertion description "[Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_provenance.