http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#head http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#assertion http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#provenance http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#assertion http://rdf.disgenet.org/resource/gda/DGNb86cbc29c48fb9dedc65ca10ab12ed47 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/668 http://rdf.disgenet.org/resource/gda/DGNb86cbc29c48fb9dedc65ca10ab12ed47 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0025322 http://rdf.disgenet.org/resource/gda/DGNb86cbc29c48fb9dedc65ca10ab12ed47 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#provenance http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#assertion http://purl.org/dc/terms/description [Blepharophimosis 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 FOXL2, a putative forkhead transcription factor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/12529855 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/dc/terms/created 2017-10-17T13:10:58+02:00 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP122679.RA5MlOfht0olaFKjK1mf7insOCensEVBX-w-mttwl9cxo http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0