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- source_evidence_literature type ECO_0000212 NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_assertion description "[In a group of 36 Mexican mestizo patients with MPN, we studied five molecular markers: The BCR/ABL1 fusion gene, the JAK2 V617F mutation, the JAK2 exon 12 mutations, the MPL W515L mutation and the MPL W515K mutation; 17 patients with essential thrombocythemia (ET), eight with polycythemia vera (PV), four with primary mielofibrosis (MF), five with undifferentiated MPN, one with primary erythrocytosis and one with familial thrombocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_assertion evidence source_evidence_literature NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_assertion SIO_000772 19843380 NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_assertion wasDerivedFrom befree-2016 NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_assertion wasGeneratedBy ECO_0000203 NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.
- befree-2016 importedOn "2016-02-19" NP770415.RAUuNHKeS0q2Af7DCPxKvNEvordpFvLe2JFChLx4qrj3o130_provenance.