Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_assertion description "[NUP98-HOXD13 (NHD13) fusions have been identified in patients with myelodysplastic syndrome, acute myelogenous leukemia and chronic myeloid leukemia blast crisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_assertion evidence source_evidence_literature NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_assertion SIO_000772 17377591 NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_assertion wasDerivedFrom befree-20140225 NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_assertion wasGeneratedBy ECO_0000203 NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP844969.RAGVTN003OS62qn1a5hT84hH7eXy5kEax0FeEVb09JZLY130_provenance.