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- source_evidence_literature type ECO_0000212 NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_assertion description "[Although signalling deregulation is involved in CMML, transcriptional deregulation seems to play a pivotal role, with mutation of RUNX1, ASXL1 or TET2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_assertion evidence source_evidence_literature NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_assertion SIO_000772 20955399 NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_assertion wasDerivedFrom befree-20150227 NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_assertion wasGeneratedBy ECO_0000203 NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285051.RAsnXVrloomdwzUx6wK6Rr37l8E1_YycpsMIL_Th1ETl4130_provenance.