Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_assertion description "[Fusion of the nucleoporin gene, NUP98, and the putative RNA helicase gene, DDX10, by inversion 11 (p15q22) chromosome translocation in a patient with etoposide-related myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_assertion evidence source_evidence_literature NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_assertion SIO_000772 10830185 NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_assertion wasDerivedFrom befree-20150227 NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_assertion wasGeneratedBy ECO_0000203 NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP351747.RAWM_gp0QMiaoTSbILnh4ROwcCrR5DOQtNvCXfhrkWVUY130_provenance.