Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_assertion description "[We studied a series of 53 CMML samples including 31 cases of myeloproliferative form (MP-CMML) and 22 cases of myelodysplastic forms (MD-CMML) using array-comparative genomic hybridisation (aCGH) and sequencing of 13 candidate genes including ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, PTPN11, RUNX1, TET2 and WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_assertion evidence source_evidence_literature NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_assertion SIO_000772 20880116 NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_assertion wasDerivedFrom befree-20140225 NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_assertion wasGeneratedBy ECO_0000203 NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP724863.RAwS6ZdSN7MjWpGo4D5Cc78QF1VViG96sShTr_ArIcOvU130_provenance.