Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_assertion description "[These include WAGR (for Wilms tumor, aniridia, genitourinary anomalies, and mental retardation), and Frasier and Denys-Drash syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_assertion evidence source_evidence_literature NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_assertion SIO_000772 18385267 NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_assertion wasDerivedFrom befree-2016 NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_assertion wasGeneratedBy ECO_0000203 NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.
- befree-2016 importedOn "2016-02-19" NP663795.RAVR9w1prtgcMQ_eLtV52lhJM3vHZf1ibIPcyHzOxHxLM130_provenance.