Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_assertion description "[In particular, ASXL1 mutations are common in patients with hematologic malignancies associated with myelodysplasia, including myelodysplastic syndromes (MDSs), and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_assertion evidence source_evidence_literature NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_assertion SIO_000772 24216483 NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_assertion wasDerivedFrom befree-2016 NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_assertion wasGeneratedBy ECO_0000203 NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1126953.RAOpLysRNGKLIpQyJc1RbrjpgP6h9uX_rG9sySdXKd3Qs130_provenance.