Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_assertion description "[Mutations in inverted formin, FH2, and WH2 domain containing (INF2) are common causes of dominant focal segmental glomerulosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_assertion evidence source_evidence_literature NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_assertion SIO_000772 22961558 NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_assertion wasDerivedFrom befree-20140225 NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_assertion wasGeneratedBy ECO_0000203 NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP348459.RA2Iw94k71I9h-GrrtAWC71deDCdEceenDFq550XI5aIQ130_provenance.