http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#head http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#assertion http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#provenance http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#assertion http://rdf.disgenet.org/resource/gda/DGNbf4afda6e2a785f58eaf2def0b2a6163 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4204 http://rdf.disgenet.org/resource/gda/DGNbf4afda6e2a785f58eaf2def0b2a6163 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0035372 http://rdf.disgenet.org/resource/gda/DGNbf4afda6e2a785f58eaf2def0b2a6163 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#provenance http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#assertion http://purl.org/dc/terms/description [A number of animal models with complete or partial lack of MeCP2 functions have been generated to correlate the clinical phenotype of Rett syndrome, and studies involving different mutations of MeCP2 have shown similar effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#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/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/23912219 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#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/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/dc/terms/created 2017-10-17T13:14:29+02:00 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP676623.RA2CgKzRTkfCrRb_AQT5CPHtTWqbHw_-8hidf_rXRm5mc 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