Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_assertion wasGeneratedBy ECO_0000203 NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_assertion wasDerivedFrom befree-20150227 NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_assertion SIO_000772 19641190 NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_assertion evidence source_evidence_literature NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.
- NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_assertion description "[We report 2 novel, cryptic chromosomal abnormalities in precursor B-cell acute lymphoblastic leukemia (BCP-ALL): a translocation, either t(X;14)(p22;q32) or t(Y;14)(p11;q32), in 33 patients and an interstitial deletion, either del(X)(p22.33p22.33) or del(Y)(p11.32p11.32), in 64 patients, involving the pseudoautosomal region (PAR1) of the sex chromosomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974551.RAsuo1bkOXoI-t_-ajmX6iIb7IPW0njOoJ2w1dF9c89iU130_provenance.