Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_assertion description "[We carried out a genome-wide association study (GWAS) by genotyping 620 390 single-nucleotide polymorphisms (SNPs) in a case-control sample of Norwegian origin (the TOP study) including bipolar disorder (n=194), healthy controls (n=336) and schizophrenia (n=230), followed by replication and combined analysis in a genetically concordant Icelandic sample of bipolar disorder (n=435), and healthy controls (n=10,258).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_assertion evidence source_evidence_literature NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_assertion SIO_000772 20451256 NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_assertion wasDerivedFrom befree-20150227 NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_assertion wasGeneratedBy ECO_0000203 NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1004864.RAmSGVudyLaLD9zUvpvA71uLQ0AtbQgaTqB7waesLe2E8130_provenance.