Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion description "[Minimal change disease (MCD) is the most common cause of nephrotic syndrome in children and is associated with the expression of CD80 in podocytes and the increased excretion of CD80 in urine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion evidence source_evidence_literature NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion SIO_000772 23689904 NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion wasDerivedFrom befree-2016 NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_assertion wasGeneratedBy ECO_0000203 NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1079176.RAlAGAoQ_dCGNad_gxufmAtn0uEQ1lV53pTwMpYgdNC5U130_provenance.