Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_assertion description "[In 4 CLL cases with unmutated VH genes, a common minimal 3.5-Mb gain of 2p16 spanning the REL and BCL11A oncogenes was identified, implicating these genes in the pathogenesis of CLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_assertion evidence source_evidence_literature NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_assertion SIO_000772 17053054 NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_assertion wasDerivedFrom befree-20140225 NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_assertion wasGeneratedBy ECO_0000203 NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP585544.RA-FKSmAgzemEY3BoN44OOv_IDd6W6dC0jDYZH9SVX_Kc130_provenance.