Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_assertion wasGeneratedBy ECO_0000203 NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_assertion wasDerivedFrom befree-2016 NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_assertion SIO_000772 8639909 NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_assertion evidence source_evidence_literature NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.
- NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_assertion description "[Our results indicate that the association between the t(12;21) and the deletion of the nontranslocated allele of TEL is among the most frequent abnormalities observed in B-lineage ALLs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1350341.RAn2_nLQdlWtSWZGWrVkS-9qiw9pkdY-iFJ7E_EMcj3BE130_provenance.