Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_assertion wasGeneratedBy ECO_0000203 NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_assertion wasDerivedFrom befree-20150227 NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_assertion SIO_000772 8180390 NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_assertion evidence source_evidence_literature NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.
- NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_assertion description "[Our results show that APL patients with cytogenetically normal chromosomes 15 and 17 may, nevertheless, have involvement of both PML and RARA genes defining a subgroup of APL, t(15;17)-negative/PML-RARA-positive which is analogous to Philadelphia chromosome-negative/BCR-ABL-positive CML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219219.RAPzqIZ3eUEUCgfRet-Oc1wOP-sq-b0eMM-P5Pkj3zBfc130_provenance.