Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_assertion description "[NUP98 is fused to PMX1 homeobox gene in human acute myelogenous leukemia with chromosome translocation t(1;11)(q23;p15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_assertion evidence source_evidence_literature NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_assertion SIO_000772 10397741 NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_assertion wasDerivedFrom befree-20140225 NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_assertion wasGeneratedBy ECO_0000203 NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP834474.RAAF-TetlvmoEFTVakRVslyFdDzZqvCAF8Al95m99SD7c130_provenance.