Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_assertion description "[Novel NUP98-HOXC11 fusion gene resulted from a chromosomal break within exon 1 of HOXC11 in acute myeloid leukemia with t(11;12)(p15;q13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_assertion evidence source_evidence_literature NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_assertion SIO_000772 12183408 NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_assertion wasDerivedFrom befree-20150227 NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_assertion wasGeneratedBy ECO_0000203 NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463191.RAEZCQNiU5X7ikOIf1WINuzEMEfT3x9GFl7UAYQVjTUJk130_provenance.