Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_assertion> ?p ?o ?g. }
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- NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_assertion type Assertion NP782638.RA8aOb3uA2P445HN1XfsTC42JmEFU2Y2OajFqfZNeoJ2s130_head.
- 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.