Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_assertion description "[With the exception of five persistent LGL expansions in which the granular lymphocytes did not express NKa determinants (designated LGL+NKa-), the remaining 87 cases could be phenotypically grouped according to their primary abnormality as CD8+NKa+ (n = 33), CD4+ NKa+ (n = 14), CD8dim+NKa+ (n = 7) or CD8-NKa+ (n = 33).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_assertion evidence source_evidence_literature NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_assertion SIO_000772 8485057 NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_assertion wasDerivedFrom befree-20140225 NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_assertion wasGeneratedBy ECO_0000203 NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.
- befree-20140225 importedOn "2014-02-25" NP755866.RAH1TNfnPmqVz7oH89VWThLBWcDDSTStwtIXNdTjNnV30130_provenance.