Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_assertion description "[A common genetic variation at chromosome band 6p22 is associated with susceptibility to neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_assertion evidence source_evidence_literature NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_assertion SIO_000772 18463370 NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_assertion wasDerivedFrom gad-20150221 NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_assertion wasGeneratedBy ECO_0000203 NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP155168.RAVp18f7lZ8G-XxV6m96K1WXB77BVmkt3w1YdXI9ARBoE130_provenance.