Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_assertion wasGeneratedBy ECO_0000203 NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_assertion wasDerivedFrom befree-20150227 NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_assertion SIO_000772 10931000 NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_assertion evidence source_evidence_literature NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.
- NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_assertion description "[Generation of the NUP98-HOXD13 fusion transcript by a rare translocation, t(2;11)(q31;p15), in a case of infant leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463358.RAnbuhGTMHd3IBbnm3jE4SkW1zLZEp3Xc9BgWEKGBS_d4130_provenance.