Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_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." NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_assertion evidence source_evidence_literature NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_assertion SIO_000772 15450400 NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_assertion wasDerivedFrom befree-20140225 NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_assertion wasGeneratedBy ECO_0000203 NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP448244.RAl7WOO1uLa1V1Siu0TJ3AwPv7MEoxCprDf2_k9whHuuE130_provenance.