Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_assertion description "[2 SNPs at positions -110 & -8 from translation start, in the promoter region & 5'UTR of PSMA6 were analyzed; genotype -8CG was more frequent in type 2 diabetes patients & haplotype C-110/G-8, compared to C-110/C-8 was associated with higher risk of NIDDM ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_assertion evidence source_evidence_literature NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_assertion SIO_000772 17555133 NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_assertion wasDerivedFrom lhgdn-20090331 NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_assertion wasGeneratedBy ECO_0000203 NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP135593.RA_Cccq4hIx13DTiqHDXyEcClg3JdXgKMTtbEZjQa4P70130_provenance.