Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_assertion description "[Thus, 17 cases of lymph node-based LPL were studied with fluorescence immunophenotypic and interphase cytogenetics for the investigation of neoplasia (FICTION) using a CD79a antibody and probes to detect trisomies of chromosomes 3 (15 cases), 12 (16 cases), and 18 (17 cases); rearrangements (R) of IgH (10 cases), BCL6 (6 cases), PAX5 (7 cases), and MALT1 (16 cases); and deletion 6q21 (7 cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_assertion evidence source_evidence_literature NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_assertion SIO_000772 18670352 NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_assertion wasDerivedFrom befree-20140225 NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_assertion wasGeneratedBy ECO_0000203 NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP877866.RAeh65GXmxCK4N3jOu1UME7H6l4X0PwiaflTq6eXTIFMU130_provenance.