Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_assertion description "[Chromosomal alterations and mutation of FLT3 (FMS-like tyrosine kinase 3) tyrosine kinase receptor are the frequent genetic alterations in acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_assertion evidence source_evidence_literature NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_assertion SIO_000772 22562027 NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_assertion wasDerivedFrom befree-20140225 NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_assertion wasGeneratedBy ECO_0000203 NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP180499.RArZVgzlZRK40Ad4nHpfz7S-8sY-WchHGw1MdZYBCbyBI130_provenance.