http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#head http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#assertion http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#provenance http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#assertion http://rdf.disgenet.org/resource/gda/DGNf705d1c3c21cfa7909dabdc008d962f1 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/9839 http://rdf.disgenet.org/resource/gda/DGNf705d1c3c21cfa7909dabdc008d962f1 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1856113 http://rdf.disgenet.org/resource/gda/DGNf705d1c3c21cfa7909dabdc008d962f1 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#provenance http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#assertion http://purl.org/dc/terms/description [Mowat-Wilson syndrome (MWS) is a genetic disease caused by heterozygous mutations or deletions of the ZEB2 gene and is characterized by distinctive facial features, epilepsy, moderate to severe intellectual disability, corpus callosum abnormalities and other congenital malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#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/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/23322667 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#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/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/dc/terms/created 2017-10-17T13:17:49+02:00 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1198281.RAh3FKf0-figvSr1ozYBmBvUIBI94m2v2h3Cu6UraycCw 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