Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_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." NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_assertion evidence source_evidence_literature NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_assertion SIO_000772 21521299 NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_assertion wasDerivedFrom befree-2016 NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_assertion wasGeneratedBy ECO_0000203 NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.
- befree-2016 importedOn "2016-02-19" NP889772.RAx3LXK6Ptcs95116-pZWCPNxHtsZqQ3eZf6c0bgGD-KU130_provenance.