Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_assertion description "[The genomic typing for DRB1, DRB3, DRB4, DRB5, DQA1, DQB1 and DPB1 genes revealed an increased frequency of the DRB1*0701; DQA1*0201; DQB1*0201 haplotype (23.5 vs 9.9% of the controls) and of DPB*0201 allele (42.3 vs 13.2% of controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_assertion evidence source_evidence_literature NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_assertion SIO_000772 7483776 NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_assertion wasDerivedFrom befree-2016 NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_assertion wasGeneratedBy ECO_0000203 NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1308398.RA_TAO9Bl_wUrz8ZpnwjCA5c_o2YJZPMKaYw3jO78UOgo130_provenance.