Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_assertion description "[The t(12;21) is a recurring chromosomal abnormality in acute lymphoblastic leukaemias (ALLs) which results in the production of an ETV6-AML1 fusion gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_assertion evidence source_evidence_literature NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_assertion SIO_000772 9233592 NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_assertion wasDerivedFrom befree-20150227 NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_assertion wasGeneratedBy ECO_0000203 NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284925.RAGd_uDB7A2KtGPftIfS3V_eeQSB_CcRZwXNVQASz294I130_provenance.