Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_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." NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_assertion evidence source_evidence_literature NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_assertion SIO_000772 21932610 NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_assertion wasDerivedFrom befree-2016 NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_assertion wasGeneratedBy ECO_0000203 NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.
- befree-2016 importedOn "2016-02-19" NP925050.RAY2UHg1D_iFj6N5EIe8TvlzgRXcsg-sJ8xDC4LG1ArIw130_provenance.