Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_assertion wasGeneratedBy ECO_0000203 NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_assertion wasDerivedFrom befree-20140225 NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_assertion SIO_000772 11875049 NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_assertion evidence source_evidence_literature NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_assertion description "[Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP713621.RAepcf0iWWhhH4_XbYA9eJJLDA19Q6xD9qa2cYsvSnbRk130_provenance.