Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_assertion description "[The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_assertion evidence source_evidence_literature NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_assertion SIO_000772 11810292 NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_assertion wasDerivedFrom befree-20140225 NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_assertion wasGeneratedBy ECO_0000203 NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP168888.RAXQja6O4EpYze0OeDBbJNGm0y4BP3ZzRLIfHt6XKrnPc130_provenance.