Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_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." NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_assertion evidence source_evidence_literature NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_assertion SIO_000772 12183408 NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_assertion wasDerivedFrom befree-20140225 NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_assertion wasGeneratedBy ECO_0000203 NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP154676.RAVJ5ku55F4RnxjoEdPNM9kAtITYNB9wUgl7B64abQYxg130_provenance.