Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_assertion description "[To assess the variation between detection methods in the interpretation of a submicroscopic gene deletion, we performed an extra signal (ES)-FISH BCR/ABL and double-FISH (D-FISH) BCR/ABL on frozen bone marrow cells from 79 patients with CML (63 in the chronic phase, 6 in the accelerated phase, and 10 in blast crisis) and 30 patients with a BCR/ABL-negative myeloproliferative disorder as determined by RT-PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_assertion evidence source_evidence_literature NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_assertion SIO_000772 15723338 NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_assertion wasDerivedFrom befree-2016 NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_assertion wasGeneratedBy ECO_0000203 NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.
- befree-2016 importedOn "2016-02-19" NP481802.RAVQbmNCVfO1UX4vxCruhgi0171vzBaSqZWU2W7k90Rls130_provenance.