Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_assertion description "[The aim of this study was to establish the frequency of combinatorial and separate copy number changes of INK4A (9p21), erbB-1 (7p11), erbB-2 (17q17-21), CMYC (8q24), CCND1 (11q13) and ZNF217 (20q13) in urothelial tumors; a tissue microarray of 159 urothelial bladder tumors was analyzed by fluorescence in situ hybridization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_assertion evidence source_evidence_literature NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_assertion SIO_000772 15897688 NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_assertion wasDerivedFrom befree-2016 NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_assertion wasGeneratedBy ECO_0000203 NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.
- befree-2016 importedOn "2016-02-19" NP495172.RAwjv97SA_dGKAlCCws-n4M3bdVCZJIgo22itvAAjK0cU130_provenance.