Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_assertion description "[FOXP2 (>10% nuclear positivity) was detectable in 90.2% of MM (55/61) and 90.9% of MGUS (10/11) patients, showing more frequent expression than CD56 and labelling 75% of CD56-negative MM (9/12).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_assertion evidence source_evidence_literature NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_assertion SIO_000772 20096010 NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_assertion wasDerivedFrom befree-2016 NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_assertion wasGeneratedBy ECO_0000203 NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.
- befree-2016 importedOn "2016-02-19" NP788855.RAYTMHkO2DuJ4-ja2mvGie_lJxEOyJeDfEZjlGalG2dcY130_provenance.