Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_assertion description "[Recurrent genetic abnormalities in B-lymphoblastic leukemia with prognostic significance are well known and specifically delineated in the WHO 2008 classification (eg hyperdiploidy, t(9;22)(q34;q11.2); BCR-ABL1, t(12;21)(p13;q22); ETV6-RUNX1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_assertion evidence source_evidence_literature NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_assertion SIO_000772 21822204 NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_assertion wasDerivedFrom befree-20150227 NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_assertion wasGeneratedBy ECO_0000203 NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387088.RAJmw8DgnWj9SN7ijs-btyFQsjMwpwAWumvjc3COe7U08130_provenance.