Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_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." NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_assertion evidence source_evidence_literature NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_assertion SIO_000772 22214819 NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_assertion wasDerivedFrom befree-20140225 NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_assertion wasGeneratedBy ECO_0000203 NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP754522.RAFpiZYiIeDoQC3RZ0uoCXAwBNT34fDHZF2A6acJWX6LI130_provenance.