Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_assertion description "[We have investigated the incidence of 13q14 deletions in a series of 74 SLVL cases by interphase fluorescence in situ hybridization using unique sequence probes for the RB1 and the D13S25 loci, which are frequently deleted in chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_assertion evidence source_evidence_literature NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_assertion SIO_000772 9563492 NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_assertion wasDerivedFrom befree-20140225 NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_assertion wasGeneratedBy ECO_0000203 NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP408506.RAwGIWuGDnMI96CJjfZS45OumZDO0jZgD3fvwpmBI-4N4130_provenance.