Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_assertion description "[These data show that the 1;19 translocation consistently results in exchange of 3' exons encoding the HLH motifs of E2A with DNA from chromosome 1 to form a fusion gene on the derivative 19 chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_assertion evidence source_evidence_literature NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_assertion SIO_000772 2078515 NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_assertion wasDerivedFrom befree-20140225 NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_assertion wasGeneratedBy ECO_0000203 NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651405.RAHoOjn1nxhTQBq0ZyYCMRviV7Udv0Sn3LtyF-RwAK5qI130_provenance.