Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_assertion description "[The purpose of this study was to investigate the cytogenetic abnormalities present in a series of 13 CD30+ CTCL samples obtained from nine patients fulfilling both EORTC and WHO diagnostic criteria, by the use of comparative genomic hybridization (CGH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_assertion evidence source_evidence_literature NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_assertion SIO_000772 14595754 NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_assertion wasDerivedFrom befree-20150227 NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_assertion wasGeneratedBy ECO_0000203 NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP292120.RAcYUJX0HA41bCo3yo1VjeRD7DYa7C3B2qsVqWVaBltXE130_provenance.