Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_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." NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_assertion evidence source_evidence_literature NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_assertion SIO_000772 22606303 NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_assertion wasDerivedFrom befree-20150227 NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_assertion wasGeneratedBy ECO_0000203 NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.
- befree-20150227 importedOn "2015-02-27" NP600976.RApmDifLIi_NwLQXyQ4d97GC6WgQjcUQ1BZ2xY9jppMio130_provenance.