Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion description "[Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion evidence source_evidence_literature NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion SIO_000772 21911584 NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion wasDerivedFrom befree-20140225 NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_assertion wasGeneratedBy ECO_0000203 NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP642339.RAiHG-tiH91aMv3YbB9uMO25BdJ0gplDUrylQuX9Mxg6w130_provenance.