Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_assertion description "[Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), an autosomal dominant syndrome in which an eyelid malformation is associated (type I) or not (type II) with premature ovarian failure (POF), has recently been ascribed to mutations in the forkhead transcription factor 2 (FOXL2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_assertion evidence source_evidence_literature NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_assertion SIO_000772 15450400 NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_assertion wasDerivedFrom befree-20140225 NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_assertion wasGeneratedBy ECO_0000203 NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP860507.RAUQddGfIUgSoqFBeez00onaVKUKA4jT79UG-18vQY7iQ130_provenance.