Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_assertion description "[The frequency of the A allele of P12A polymorphism was 0.16 and the t allele of c1431t polymorphism, 0.13 in patients with type 2 diabetes, and 0.13 and 0.12 respectively in subjects without diabetes 3.2% of patients with and 1.4% without type 2 diabetes were A12A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_assertion evidence source_evidence_literature NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_assertion SIO_000772 11409297 NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_assertion wasDerivedFrom befree-20150227 NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_assertion wasGeneratedBy ECO_0000203 NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP911842.RA1BOHRWI5UXr4mn3dXxk-bgiqp5h4QNTlQBbgqxVZVE0130_provenance.