Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_assertion description "[In contrast to nonconsanguineous pedigrees, mutations in EIF2AK3 are the most common known genetic cause of diabetes among patients born to consanguineous parents (24 vs. < 2%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_assertion evidence source_evidence_literature NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_assertion SIO_000772 19837917 NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_assertion wasDerivedFrom befree-2016 NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_assertion wasGeneratedBy ECO_0000203 NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.
- befree-2016 importedOn "2016-02-19" NP769946.RANpAQa5U4y0r4GlIJAkCv_Pt4c6Oo1oeUmnODOcC14Uk130_provenance.