Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_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." NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_assertion evidence source_evidence_literature NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_assertion SIO_000772 12115499 NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_assertion wasDerivedFrom befree-20150227 NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_assertion wasGeneratedBy ECO_0000203 NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP686186.RASECxnd6wo-NgPLK9iogYSIgLObZmnYlcS93M1tANLmk130_provenance.