Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_assertion wasGeneratedBy ECO_0000203 NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_assertion wasDerivedFrom befree-20150227 NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_assertion SIO_000772 16384941 NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_assertion evidence source_evidence_literature NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.
- NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_assertion description "[The coding sequence and flanking intron/exon junctions of IMPDH1 were analyzed in 203 patients with autosomal dominant RP (adRP), 55 patients with autosomal recessive RP (arRP), 7 patients with isolated RP, 17 patients with macular degeneration (MD), and 24 patients with Leber congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509523.RAzO4s3Eg7cmPDw8Ax8UD9iQyEmkAtcS_GUgb5PPpYQdA130_provenance.