Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_assertion description "[To report novel spectral domain optical coherence tomography (SD-OCT) findings and new mutational data in patients with 'cone dystrophy with supernormal rod electroretinogram', a recessive childhood onset retinal dystrophy consequent upon mutation in the KCNV2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_assertion evidence source_evidence_literature NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_assertion SIO_000772 21558291 NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_assertion wasDerivedFrom befree-2016 NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_assertion wasGeneratedBy ECO_0000203 NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP892995.RAMlrYXVmZCbIdZMn5gG2nA-Z92BZRPKwP9IckSIL6CTQ130_provenance.