Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- befree-2016 importedOn "2016-02-19" NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_assertion wasGeneratedBy ECO_0000203 NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_assertion wasDerivedFrom befree-2016 NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_assertion SIO_000772 14506644 NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_assertion evidence source_evidence_literature NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.
- NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_assertion description "[These findings suggest that an NPM/MLF1 fusion is the primary molecular abnormality in t(3;5) MDS and AML with multilineage dysplasia, and also that cases with NPM/MLF1 may be clinically distinct from other MDS-associated disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414292.RA43lxGu9uH8hSMFrcK7r7t55Mq0by9ezHiLqufYb-rmI130_provenance.