Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_assertion description "[No or only very faint signals were obtained in HL for CXCL12, CCL7 and CCL8, but CXCL10, CCL5, CCL13, CCL17 and CCL22 were highly or differentially expressed in HL cell lines and tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_assertion evidence source_evidence_literature NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_assertion SIO_000772 12115499 NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_assertion wasDerivedFrom befree-20150227 NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_assertion wasGeneratedBy ECO_0000203 NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP686907.RAAueBQCjYLWRkOI4cqYIy54YdutemstD-6JpK4OcymoI130_provenance.