Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_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." NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_assertion evidence source_evidence_curated NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_assertion SIO_000772 11810292 NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_assertion wasDerivedFrom ctd_human-20130708 NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_assertion wasGeneratedBy ECO_0000218 NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP29867.RAdYmC9I_hw28Ab2J_P1g6YDY9T4n8eQlE7LWT5SKdwUA130_provenance.