Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_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." NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_assertion evidence source_evidence_literature NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_assertion SIO_000772 15450400 NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_assertion wasDerivedFrom befree-20150227 NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_assertion wasGeneratedBy ECO_0000203 NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP270283.RAYESQTTo9v0e0P1eaKqFbcNhLx6i6HX1kSr1DCYsqbfY130_provenance.