Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_assertion description "[Major form of NUP98/HOXC11 fusion in adult AML with t(11;12)(p15;q13) translocation exhibits aberrant trans-regulatory activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_assertion evidence source_evidence_literature NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_assertion SIO_000772 12970787 NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_assertion wasDerivedFrom befree-20140225 NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_assertion wasGeneratedBy ECO_0000203 NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.
- befree-20140225 importedOn "2014-02-25" NP802122.RAIwCBoOM88BVPVQXI632ChKeP51Lzc3cUtHXQD6KGOag130_provenance.