Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_assertion description "[In humans, inactivating mutations in GLUT2 cause Fanconi-Bickel syndrome, which is characterised by hepatomegaly and kidney disease; defects in insulin secretion are rare in adult patients, but GLUT2 mutations cause transient neonatal diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_assertion evidence source_evidence_literature NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_assertion SIO_000772 25421524 NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_assertion wasDerivedFrom befree-2016 NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_assertion wasGeneratedBy ECO_0000203 NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1239633.RAwDv8bB8vikQ9g2QLd5msNHO79K5vPIMzVstXO-jOB-U130_provenance.