Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_assertion description "[Fanconi-Bickel syndrome (FBS) is a rare autosomal recessive disorder of carbohydrate metabolism recently demonstrated to be caused by mutations in Glut2, the gene for the glucose transporter protein 2 expressed in liver, pancreas, intestine and kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_assertion evidence source_evidence_literature NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_assertion SIO_000772 9809815 NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_assertion wasDerivedFrom befree-2016 NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_assertion wasGeneratedBy ECO_0000203 NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1407787.RAQT-4WBA7HEZFxQQQ73mIGZhAaYZdWsEHTZPov3WXShU130_provenance.