Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_assertion description "[The nonrandom nature of the breakpoints in this case was confirmed by the analysis of a second independent case of T-ALL containing a t(1;7) translocation, which was also found to show breakage within the LCK locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_assertion evidence source_evidence_literature NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_assertion SIO_000772 1680958 NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_assertion wasDerivedFrom befree-20150227 NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_assertion wasGeneratedBy ECO_0000203 NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP532374.RAS6z-Q9xCpnIizMMoIHldmPjQemtDe_7j-7CrQoF7fWE130_provenance.