Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- befree-2016 importedOn "2016-02-19" NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_assertion wasGeneratedBy ECO_0000203 NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_assertion wasDerivedFrom befree-2016 NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_assertion SIO_000772 21436895 NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_assertion evidence source_evidence_literature NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.
- NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_assertion description "[Our genome-wide association study (GWAS) has identified common variants within FLJ22536, BARD1, and LMO1 as significantly associated with neuroblastoma and more robustly associated with high-risk disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP882237.RAfmVWiC99GBumzIyPtgFj70n0HS4wJTGcwNH-UDNOmww130_provenance.