Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_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." NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion evidence source_evidence_literature NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion SIO_000772 23689904 NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion wasDerivedFrom befree-20140225 NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_assertion wasGeneratedBy ECO_0000203 NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP584843.RAlPyzA9jkPejgAe04TRC7atl4-kiEWpWpnszGnxvaFFE130_provenance.