Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_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." NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_assertion evidence source_evidence_literature NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_assertion SIO_000772 11323086 NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_assertion wasDerivedFrom befree-20140225 NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_assertion wasGeneratedBy ECO_0000203 NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.
- befree-20140225 importedOn "2014-02-25" NP868768.RAlf6drCeERwQMFlvzVg6r4vxGgHUsCJT56qcQJMpv_Ro130_provenance.