Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion description "[Mutations in KCNV2 have been proposed as the molecular basis for cone dystrophy with supernormal rod electroretinogram.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion evidence source_evidence_literature NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion SIO_000772 23115240 NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion wasDerivedFrom befree-20140225 NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_assertion wasGeneratedBy ECO_0000203 NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.
- befree-20140225 importedOn "2014-02-25" NP745794.RAkffcrJegzLqV8iNwzUl4tffIXnafu6ooblTq7csU9do130_provenance.