Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_assertion description "[Mice that express a NUP98-HOXD13 (NHD13) transgene develop a MDS that closely mimics the human condition in terms of dysplasia, ineffective hematopoiesis, and transformation to acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_assertion evidence source_evidence_literature NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_assertion SIO_000772 22606303 NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_assertion wasDerivedFrom befree-20140225 NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_assertion wasGeneratedBy ECO_0000203 NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563687.RAUzk-ibaFVqvqmdUDSyp-Ey33LO2H00E3s2JWbVNJffQ130_provenance.