Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_assertion wasGeneratedBy ECO_0000203 NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_assertion wasDerivedFrom befree-2016 NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_assertion SIO_000772 7742547 NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_assertion evidence source_evidence_literature NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.
- NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_assertion description "[Clinicohematological data in these studies as well as the restriction mapping of chromosomal breakpoints strongly suggest that (1) common features in MDSs involving the TEL gene are monocytosis and eosinophilia, (2) chromosomes other than no.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1320368.RAgJFS2D_wiHSAwXuRbcDV2ylveMaSJ7WnBfgpzfhr7QY130_provenance.