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- source_evidence_literature type ECO_0000212 NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_assertion description "[We have studied the mutational status of TET2 (complete coding region), ASXL1 (exon12), IDH1 (R132), IDH2 (R140 and R172), and c-CBL (exons 8 and 9) in 62 MPN patients (52 essential thrombocythemia (ET), five polycythemia vera (PV), and five primary myelofibrosis (PMF)) negative for both JAK2 (V617F and exon 12) and MPL (exon 10) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_assertion evidence source_evidence_literature NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_assertion SIO_000772 21904853 NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_assertion wasDerivedFrom befree-2016 NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_assertion wasGeneratedBy ECO_0000203 NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.
- befree-2016 importedOn "2016-02-19" NP922475.RA2y6g4gr00pgczGWV1eyPSgV2SmA0MTERwjJCBoZ65p0130_provenance.