Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion description "[The inv(11)(p15q22), a rare but recurrent chromosome abnormality that creates a NUP98-DDX10 fusion gene, is associated with de novo or secondary myeloid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion evidence source_evidence_literature NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion SIO_000772 17116492 NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion wasDerivedFrom befree-20150227 NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_assertion wasGeneratedBy ECO_0000203 NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP351739.RAXsmGwzGpXnOcS0W7yL5o8CTsCxDtHlT-xeBazRAZRbI130_provenance.