Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_assertion description "[We subjected 13 cases of CLC to a comprehensive molecular analysis including immunohistochemistry for E-cadherin, estrogen and progesterone receptors, HER2/neu and p53; high-resolution comparative genomic hybridization (HR-CGH); microarray-based CGH (aCGH); and fluorescent and chromogenic in situ hybridization for CCND1 and FGFR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_assertion evidence source_evidence_literature NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_assertion SIO_000772 17121884 NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_assertion wasDerivedFrom befree-20140225 NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_assertion wasGeneratedBy ECO_0000203 NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP859901.RAiKapGgRgLILFJLRntrX3FJ8aeNM5mC4JApMh8izNoe0130_provenance.