Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_assertion wasGeneratedBy ECO_0000203 NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_assertion wasDerivedFrom befree-20150227 NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_assertion SIO_000772 20023659 NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_assertion evidence source_evidence_literature NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.
- NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_assertion description "[These mutations, all within the diaphanous inhibitory domain of INF2, segregate with FSGS in 11 unrelated families and alter highly conserved amino acid residues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939275.RAbwU58CCBq2NN47834AuuJikRtLKuofuRTZAwYnBXnL8130_provenance.