Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_assertion description "[We identified two patients with acute leukemia in relapse (one lymphoblastic and the other with evidence of mixed lymphoid-myeloid differentiation) with t(12;17)(p12;q11) as the primary karyotypic abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_assertion evidence source_evidence_literature NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_assertion SIO_000772 1458446 NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_assertion wasDerivedFrom befree-2016 NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_assertion wasGeneratedBy ECO_0000203 NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.
- befree-2016 importedOn "2016-02-19" NP418646.RAt9EHd0nPMhdKmwwStGJ03LWYMEdZJMSq4U_ctLG0rEM130_provenance.