Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- befree-2016 importedOn "2016-02-19" NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_assertion wasGeneratedBy ECO_0000203 NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_assertion wasDerivedFrom befree-2016 NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_assertion SIO_000772 22735794 NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_assertion evidence source_evidence_literature NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.
- NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_assertion description "[The aim of this study was to identify mutations in the TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindness (CSNB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP993241.RAtVp2MgwV_2eh_KDfr3P7rTF3nz2e7Wg4RoIEaHuRANA130_provenance.