Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_assertion description "[In a systematic tyrosine kinase gene exon resequencing study, 21 of 24 FLT3 exons were sequenced in samples from 53 patients with AML, 9 patients with acute lymphoblastic leukemia (ALL), and 3 patients with myelodysplasia samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_assertion evidence source_evidence_literature NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_assertion SIO_000772 15178581 NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_assertion wasDerivedFrom befree-20140225 NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_assertion wasGeneratedBy ECO_0000203 NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722726.RAFiw9eTR_99XfaNYeLVB1Ol3QGKP8ZPXYGzmg6yeJwco130_provenance.