Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_assertion description "[A group of 100 46,XY DSD and two POI was studied for NR5A1 mutations and their impact.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_assertion evidence source_evidence_literature NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_assertion SIO_000772 22549935 NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_assertion wasDerivedFrom befree-20140225 NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_assertion wasGeneratedBy ECO_0000203 NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP459252.RAUm57bWf0OrjB4TsAegykaG7oO9V8aCGhJSEwPERWtLs130_provenance.