Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- befree-2016 importedOn "2016-02-19" NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_assertion wasGeneratedBy ECO_0000203 NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_assertion wasDerivedFrom befree-2016 NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_assertion SIO_000772 22311941 NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_assertion evidence source_evidence_literature NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.
- NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_assertion description "[A common variant at position 801 in 3'-untranslated region in CXCL12 gene (designated CXCL12-3'G801A) has been reported in association with autoimmune diseases, such as type 1 diabetes and systemic sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959146.RA8eJ5lfGsUSMnxtQ0HEINrEk00FtmwuKW5O6eR6YqWTc130_provenance.