Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_assertion description "[Deletions from the derivative chromosome 9, der(9), of the translocation, t(9;22)(q34;q11), at the site of the ABL/BCR fusion gene, have been demonstrated by fluorescence in situ hybridisation (FISH), in both Philadelphia chromosome (Ph)-positive chronic myeloid leukaemia (CML) and acute lymphoblastic leukaemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_assertion evidence source_evidence_literature NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_assertion SIO_000772 15716990 NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_assertion wasDerivedFrom befree-2016 NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_assertion wasGeneratedBy ECO_0000203 NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.
- befree-2016 importedOn "2016-02-19" NP481294.RA05EfgUHBVQ6LWNH1w_P3cP7HKEihkvuwK4WTutWMmis130_provenance.