Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_assertion description "[Various specific chromosome rearrangements, including t(8;21), t(15;17), and inv(16), are found in acute myeloid leukemia (AML) and in childhood acute lymphocytic leukemia (ALL), t(12;21) and t(1;19) are common.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_assertion evidence source_evidence_literature NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_assertion SIO_000772 15967214 NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_assertion wasDerivedFrom befree-2016 NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_assertion wasGeneratedBy ECO_0000203 NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.
- befree-2016 importedOn "2016-02-19" NP500277.RA1dpyyFylsn3ra8WBFiu195f3IKqQ4MN5-gmWdjKivx0130_provenance.