Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_assertion description "[Detection of cryptic and variant IGH-MYC rearrangements in high-grade non-Hodgkin's lymphoma by fluorescence in situ hybridization: implications for cytogenetic testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_assertion evidence source_evidence_literature NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_assertion SIO_000772 20303018 NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_assertion wasDerivedFrom befree-2016 NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_assertion wasGeneratedBy ECO_0000203 NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP801138.RAej4UO34dhGqLFpsWSTi1x6XO_D-X9b3JjKpr3Khdb7Y130_provenance.