Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_assertion description "[Somatic TET2 mutations are frequently observed in myelodysplastic syndromes (MDS), myeloproliferative neoplasms (MPN), MDS/MPN overlap syndromes including chronic myelomonocytic leukaemia (CMML), acute myeloid leukaemias (AML) and secondary AML (sAML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_assertion evidence source_evidence_literature NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_assertion SIO_000772 21057493 NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_assertion wasDerivedFrom befree-20150227 NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_assertion wasGeneratedBy ECO_0000203 NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914161.RA_K4g8hOTHV3M5EwVTESiqiwKQnqOcYm1WqkQX7VF4Y0130_provenance.