Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_assertion description "[it is reported for the first time that mutations in CABP4 lead to autosomal recessive congenital stationary night blindness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_assertion evidence source_evidence_literature NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_assertion SIO_000772 16960802 NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_assertion wasDerivedFrom lhgdn-20090331 NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_assertion wasGeneratedBy ECO_0000203 NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP219520.RANFPq4Xy8P_scPC4kPEkj3lJwKcMigOGjxx2s6OiY2w0130_provenance.