Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_assertion description "[Fine-tiling array comparative genomic hybridization of MYCN amplicons from neuroblastoma (NB) cell lines and primary tumors revealed that 56.5% of the amplicons cluster in FRA2C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_assertion evidence source_evidence_literature NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_assertion SIO_000772 21258086 NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_assertion wasDerivedFrom befree-20140225 NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_assertion wasGeneratedBy ECO_0000203 NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478044.RAcCPtFtUvCTOcWNe7wi0B1Qpoa8UfNiYSIC2A2SSLdaU130_provenance.