Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_assertion description "[We have used comparative genomic hybridization to identify genome copy number changes that can predict outcome in patients with stage IV neuroblastoma without MYCN amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_assertion evidence source_evidence_literature NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_assertion SIO_000772 18765546 NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_assertion wasDerivedFrom befree-20150227 NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_assertion wasGeneratedBy ECO_0000203 NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP582640.RAgC_Mmx3TrRVcVBhtsG2DjEUZyiezYA35QNCWWlz_F3g130_provenance.