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- source_evidence_literature type ECO_0000212 NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_assertion description "[The development of novel technologies, such as massively parallel DNA sequencing, has led to the identification of several novel recurrent gene mutations, such as DNA methyltransferase (Dnmt)3a, ten-eleven-translocation oncogene family member 2 (TET2), isocitrate dehydrogenase (IDH)1/2, additional sex comb-like 1 (ASXL1), enhancer of zeste homolog 2 (EZH2) and ubiquitously transcribed tetratricopeptide repeat X chromosome (UTX) mutations in acute myeloid leukemia (AML) and other myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_assertion evidence source_evidence_literature NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_assertion SIO_000772 23760684 NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_assertion wasDerivedFrom befree-20150227 NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_assertion wasGeneratedBy ECO_0000203 NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP388746.RApXOSqO3AOXPJdJoVJ1Dxd83hU1JzSQDVuDDo5NoUgiw130_provenance.