Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_assertion description "[Using a NUP98-HOXD13 fusion gene, we have developed a mouse model that faithfully recapitulates all of the key features of MDS, including peripheral blood cytopenias, bone marrow dysplasia, and apoptosis, and transformation to acute leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_assertion evidence source_evidence_literature NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_assertion SIO_000772 15755899 NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_assertion wasDerivedFrom befree-2016 NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_assertion wasGeneratedBy ECO_0000203 NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP484735.RAeM5ShCGUxk7wg6GYvjd6r4W-75JGBwcByCdS6d0_VBQ130_provenance.