Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_assertion description "[To describe patients with cone dystrophy and supernormal rod electroretinogram (ERG) and search for mutations in the recently described KCNV2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_assertion evidence source_evidence_literature NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_assertion SIO_000772 18400204 NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_assertion wasDerivedFrom befree-20140225 NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_assertion wasGeneratedBy ECO_0000203 NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.
- befree-20140225 importedOn "2014-02-25" NP689669.RAYiGvsUzPiRB-K470zdd5qa5oL7Z5Mm3KOtnmccGdlig130_provenance.