Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion wasGeneratedBy ECO_0000203 NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion wasDerivedFrom befree-20150227 NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion SIO_000772 22619094 NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion evidence source_evidence_literature NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.
- NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion description "[These findings indicate that the distribution of NOTCH1 mutations in CLL with trisomy 12 is heterogeneous and that the presence of additional chromosomal abnormalities such as trisomy 18 could change the prognosis of these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance.