Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_assertion description "[Five single nucleotide polymorphisms (SNPs) at chromosome 3q28, ALPK1, FAM78B, and UMODL1 were significantly (false discovery rate<0.05) associated with CKD by the GWAS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_assertion evidence source_evidence_literature NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_assertion SIO_000772 23539754 NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_assertion wasDerivedFrom befree-2016 NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_assertion wasGeneratedBy ECO_0000203 NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1064870.RAgZcby7JHsfsjfxnQJr-gL4ncaSYxxDL55jrNUjjDyfM130_provenance.