Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_assertion wasGeneratedBy ECO_0000203 NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_assertion wasDerivedFrom befree-2016 NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_assertion SIO_000772 23372056 NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_assertion evidence source_evidence_literature NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.
- NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_assertion description "[We determined the fraction of families in a well-characterized cohort with a provisional diagnosis of autosomal dominant retinitis pigmentosa (adRP) that have disease-causing mutations in the X-linked retinitis pigmentosa GTPase regulator (RPGR) gene or the retinitis pigmentosa 2 (RP2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1049086.RA18gF6b5rZg7kMgyx-vWYi5eIGxF2o5mk6MIdZrCYmqM130_provenance.