Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_assertion wasGeneratedBy ECO_0000203 NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_assertion wasDerivedFrom befree-20150227 NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_assertion SIO_000772 7742547 NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_assertion evidence source_evidence_literature NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.
- NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_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." NP387403.RABggUqqn7IVW1XIVQSG8oAitD4_1LhCjEx0MVr3FOkvM130_provenance.