Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_assertion description "[We report a rare cryptic ins(12;9)(p13;q34q34), a chromosomal abnormality involving the ABL1 (9q34) and the ETV6 (alias TEL; 12p13) genes, detectable only by fluorescence in situ hybridization (FISH), in a patient with Philadelphia-negative chronic myeloid leukemia (CML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_assertion evidence source_evidence_literature NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_assertion SIO_000772 19480935 NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_assertion wasDerivedFrom befree-2016 NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_assertion wasGeneratedBy ECO_0000203 NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP741944.RAHz0BEmuoSDs6G8aLPQ2zFy_TDdcaR826dIf_6ev2GBQ130_provenance.