Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_assertion description "[We genotyped ASXL1 and up to 18 other genes including epigenetic (TET2, EZH2, IDH1, IDH2, DNMT3A), splicing (SF3B1, SRSF2, ZRSF2, U2AF1), transcription (RUNX1, NPM1, TP53), and signaling (NRAS, KRAS, CBL, JAK2, FLT3) regulators in 312 patients with CMML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_assertion evidence source_evidence_literature NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_assertion SIO_000772 23690417 NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_assertion wasDerivedFrom befree-20150227 NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_assertion wasGeneratedBy ECO_0000203 NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978491.RAKyv7bHUQ6mpDLP8kSEkULirI_AkzJ4iXcr0bPf-qCRg130_provenance.