Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_assertion description "[One single nucleotide polymorphism (SNP) at codon 287 (GGG to GGT) was found in the gene and the frequency was similar among MODY/early-onset diabetes, late-onset diabetes and control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_assertion evidence source_evidence_literature NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_assertion SIO_000772 11323086 NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_assertion wasDerivedFrom befree-20150227 NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_assertion wasGeneratedBy ECO_0000203 NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1005632.RAMioJRixIXERTtvW_l9rfUpdhsVD9S_fqotdLwitNh44130_provenance.