Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_assertion description "[Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause cone dystrophy with supernormal rod electroretinogram in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_assertion evidence source_evidence_literature NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_assertion SIO_000772 16909397 NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_assertion wasDerivedFrom befree-2016 NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_assertion wasGeneratedBy ECO_0000203 NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.
- befree-2016 importedOn "2016-02-19" NP564250.RAWb5ican3nABP3e7GJc-Qx7rXelmnmK7btvsXNvRiM0s130_provenance.