Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_assertion description "[Resequencing of NTF4 revealed a nonsynonymous (A88V), silent (P151P) and two changes in the 3'UTR region, along with a known polymorphism (rs11669977) in cases of POAG; the PACG cases exhibited only the A88V variation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_assertion evidence source_evidence_literature NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_assertion SIO_000772 20463313 NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_assertion wasDerivedFrom befree-20140225 NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_assertion wasGeneratedBy ECO_0000203 NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP797825.RAhWWO5zHf7Q9tzis5QfDJC8iiAO-bbD-KXBTzKLOaEPk130_provenance.