Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_assertion description "[We then screened 200 T2D siblings/families for PSMD9 +nt460A/G, +nt437C/T and exon E197G A/G single nucleotide polymorphisms (SNPs) and performed a non-parametric linkage study to test for linkage for coronary artery disease, stroke/TIA, macro-vasculopathy and macrovascular pathology of T2D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_assertion evidence source_evidence_literature NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_assertion SIO_000772 21496327 NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_assertion wasDerivedFrom befree-20140225 NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_assertion wasGeneratedBy ECO_0000203 NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316851.RARGykrXgofPpAhiiIzsAS7UHsgMa0NO7tEmF-6nk2B4M130_provenance.