Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_assertion description "[The role of a nonsynonymous CD226 (DNAX-accessory molecule-1) variant (Gly 307Ser) in isolated Addison's disease and autoimmune polyendocrinopathy type 2 pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_assertion evidence source_evidence_literature NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_assertion SIO_000772 21521299 NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_assertion wasDerivedFrom befree-20150227 NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_assertion wasGeneratedBy ECO_0000203 NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.
- befree-20150227 importedOn "2015-02-27" NP850793.RA8idStRiecLPhAYfsaLkrtDinPyTtE_9Kq9XkM8jhDow130_provenance.