Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_assertion description "[Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) or autoimmune polyendocrine syndrome type 1 (APS-1) is a rare autosomal recessive disease caused by mutations of the AutoImmune REgulator (AIRE) gene, an important mediator of tolerance to self-antigens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_assertion evidence source_evidence_literature NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_assertion SIO_000772 21932610 NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_assertion wasDerivedFrom befree-2016 NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_assertion wasGeneratedBy ECO_0000203 NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP925049.RAcjEJCZb9JI9pegI4QxdWOI05jiQFcmTpHQXf74DFSJQ130_provenance.