Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_assertion description "[We conclude that neither the SCLL phenotype nor blood eosinophilia is a consistent feature of FGFR1-associated 8p11.2 translocations; conversely, FISH might not always reveal FGFR1 involvement in typical SCLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_assertion evidence source_evidence_literature NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_assertion SIO_000772 20143402 NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_assertion wasDerivedFrom befree-2016 NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_assertion wasGeneratedBy ECO_0000203 NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.
- befree-2016 importedOn "2016-02-19" NP792730.RA85GbBYNh0YXWzTDo_Le5waDYEHpZ__lTtVVtWieZZOg130_provenance.