Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_assertion description "[Twenty-one of 148 (14.2%) patients with CTCLs were positive for HHV7 DNA: nine of 39 (23.1%) SS, six of 14 (42.9%) CD30+ CTCLs and six of 24 (25.0%) LyP, and HHV7 DNA was negative in all 71 patients with MF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_assertion evidence source_evidence_literature NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_assertion SIO_000772 18782321 NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_assertion wasDerivedFrom befree-2016 NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_assertion wasGeneratedBy ECO_0000203 NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.
- befree-2016 importedOn "2016-02-19" NP692319.RAzmXPafe_yGFCc5f43ZH5JJjUJVGruPhPUey1KyfNisI130_provenance.