Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_assertion description "[RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_assertion evidence source_evidence_literature NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_assertion SIO_000772 18202228 NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_assertion wasDerivedFrom befree-20150227 NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_assertion wasGeneratedBy ECO_0000203 NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285404.RAWK4LO-YgXUqMVjseQ5tlMDSvyGus6ilyXGCkJZ0g7mA130_provenance.