Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_assertion description "[Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_assertion evidence source_evidence_literature NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_assertion SIO_000772 23393310 NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_assertion wasDerivedFrom befree-20140225 NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_assertion wasGeneratedBy ECO_0000203 NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP311506.RAk-U5196sxGt_VLmqmqPXEJaqP1CzmJS7ICM4Z_QlDVg130_provenance.