Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_assertion description "[In contrast with the molecular findings observed in chronic lymphocytic leukemia, our results indicate that trisomy 12 is an uncommon chromosomal aberration in SLVLs, and microdeletion of 13q14 at the RB1 locus but not D13S25 is a frequent and specific genetic event in this disease, suggesting that allelic loss of the RB1 gene may play a role in the pathogenesis of SLVL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_assertion evidence source_evidence_literature NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_assertion SIO_000772 9563492 NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_assertion wasDerivedFrom befree-20140225 NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_assertion wasGeneratedBy ECO_0000203 NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP720006.RAPYJbhu1uqgfql4X8jhAOM8igIYoZtike0WP2UIVgW2k130_provenance.