Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_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." NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_assertion evidence source_evidence_literature NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_assertion SIO_000772 19480935 NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_assertion wasDerivedFrom befree-20140225 NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_assertion wasGeneratedBy ECO_0000203 NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP649469.RAHLcKdYJ6SXQuJ71eIe9I7oS7vfsCBR95F_dI27caQ_U130_provenance.