Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_assertion description "[Fanconi-Bickel syndrome: GLUT2 mutations associated with a mild phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_assertion evidence source_evidence_literature NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_assertion SIO_000772 22214819 NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_assertion wasDerivedFrom befree-2016 NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_assertion wasGeneratedBy ECO_0000203 NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.
- befree-2016 importedOn "2016-02-19" NP950669.RAreYebs7MrD1b3krSLfNtpXlzufRfKTCj5W_x7W3ieyA130_provenance.