Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_assertion description "[The chromosomal translocation t(8;21), generating the AML1-ETO fusion protein, is frequently associated with French-American-British (FAB) type M2 acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_assertion evidence source_evidence_literature NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_assertion SIO_000772 16390317 NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_assertion wasDerivedFrom befree-20140225 NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_assertion wasGeneratedBy ECO_0000203 NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP665935.RAJnlM7ZFbmiWD4G6OPq439Ae-WQ12KrRzA6WOHHhujC0130_provenance.