Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_assertion description "[Fanconi-Bickel syndrome (FBS, OMIM #227810), a congenital disorder of carbohydrate metabolism, is caused by mutations in GLUT2 (SLC2A2), the gene encoding the glucose transporter protein-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_assertion evidence source_evidence_literature NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_assertion SIO_000772 22214819 NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_assertion wasDerivedFrom befree-20140225 NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_assertion wasGeneratedBy ECO_0000203 NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP224663.RA2Tkv_oPllC0OGbIIej2XpKF-J5LUGslqxu0pA4y5iiM130_provenance.