Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_assertion description "[Homozygous deletions of the CDKN2/CDKN2B (p15) region were detected in 10 cases (50%; 6 ALL, 2 AML, and 2 NHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_assertion evidence source_evidence_literature NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_assertion SIO_000772 7544647 NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_assertion wasDerivedFrom befree-2016 NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_assertion wasGeneratedBy ECO_0000203 NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311867.RAVJOSA4aby457xy880lTPl86R_t7rVb8YheNrsk_XU2o130_provenance.