Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_assertion description "[Nonchimeric polytransgenic 152F7 mice encompassing four human chromosome 21 genes (DSCR3, DSCR5, TTC3, and DYRK1A) within the Down syndrome critical region present with learning and memory impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_assertion evidence source_evidence_literature NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_assertion SIO_000772 17696169 NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_assertion wasDerivedFrom befree-20140225 NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_assertion wasGeneratedBy ECO_0000203 NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP869293.RA0WoyK_7QeEQOzwmoe8Brt6Q5a3dX9Ov6gcLh3MGc9kU130_provenance.