Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_assertion description "[CC abnormality rates were also compared to fluorescence in situ hybridization (FISH) results using probes for CLL (LSI D13S319/13q34/CEP 12: LSI ATM/p53).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_assertion evidence source_evidence_literature NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_assertion SIO_000772 20362231 NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_assertion wasDerivedFrom befree-20140225 NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_assertion wasGeneratedBy ECO_0000203 NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP936238.RA13D4HF7kGXdydTGLcJhSVEcaAazQYg-7FGeUiuQjNng130_provenance.