Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_assertion wasGeneratedBy ECO_0000203 NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_assertion wasDerivedFrom befree-20140225 NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_assertion SIO_000772 16931578 NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_assertion evidence source_evidence_literature NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_assertion description "[The V617F mutation is present in blood and marrow from a large proportion of patients with classic BCR/ABL-negative chronic myeloproliferative disorders and of a few patients with other clonal hematological diseases such as myelodysplastic syndrome, atypical myeloproliferative disorders, and acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP639582.RABQVDcz_cVxCtfHWTQv2dyCCDgaG7BxX6XKD-xyGr2AE130_provenance.